Varaico: Literature-Extracted Genetic Variants

Gene:OVOL2
Variant:p.S189S
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OVOL2

NM_021220.4:p.S189S

Associated Papers

SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families.

Firasat S et al.

Molecular Biology Reports, 2021

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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."