KCNV2

potassium voltage-gated channel modifier subfamily V member 2
OMIM: 607604
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Retinal Cone Dystrophy, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy