CNGA3

cyclic nucleotide gated channel alpha 3
OMIM: 600053
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Achromatopsia-2, 216900, Eye Disorders, Achromatopsia, Cone, and Cone-rod Dystrophy