CACNA2D2

calcium voltage-gated channel auxiliary subunit alpha2delta 2
OMIM: 607082
PanelMode of inheritanceDetails
1 panel
R-numbers: R59
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Absence epilepsy, Cerebellar atrophy with seizures and variable developmental delay, 618501