CNGA1

cyclic nucleotide gated channel alpha 1
OMIM: 123825
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Retinitis pigmentosa 49, RP49 (AR), Eye Disorders, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa 49, 613756