SLC24A1

solute carrier family 24 member 1
OMIM: 603617
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital Stationary Night Blindness, Night blindness, congenital stationary (complete), 1D, autosomal recessive, 613830