Varaico: Literature-Extracted Genetic Variants

Gene:SLC4A1
Variant:p.W496L
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SLC4A1

NM_000342.4:p.W496L

Associated Papers

Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein.

Ramasamy I

Bmj Case Reports, 2020

Updates on congenital hereditary endothelial dystrophy.

Mehta N et al.

Taiwan Journal of Ophthalmology, 0

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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."