Varaico: Literature-Extracted Genetic Variants

Gene:HBA2
Variant:p.A66V
Back to variants list

HBA2

NM_000517.6:p.A66V

Associated Papers

Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.

Luo H et al.

Frontiers in Genetics, 2022

Molecular classification of blood and bleeding disorder genes.

Baz B et al.

Npj Genomic Medicine, 2021

34272389 (PubMed )
Supplement: 41525_2021_228_MOESM1_ESM.pdf

Congenital erythropoietic porphyria: Recent advances.

Erwin AL et al.

Molecular Genetics and Metabolism, 2019

Ringed sideroblasts in β-thalassemia.

Cattivelli K et al.

Pediatric Blood & Cancer, 2017

Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene.

Warner CA et al.

The Journal of Clinical Investigation, 1992

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."