CACNA2D4

calcium voltage-gated channel auxiliary subunit alpha2delta 4
OMIM: 608171
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Retinal cone dystrophy 4, 610478, Congenital Stationary Night Blindness, Achromatopsia, Cone, and Cone-rod Dystrophy