Varaico: Literature-Extracted Genetic Variants

Gene:PLXNA2
Variant:p.V13V
Back to variants list

PLXNA2

NM_025179.4:p.V13V

Associated Papers

Novel intragenic deletions and point mutations of the ornithine transcarbamylase gene in congenital hyperammonemia.

Calvas P et al.

Human Mutation, 1998

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."