RAB27A

RAB27A, member RAS oncogene family
OMIM: 603868
PanelMode of inheritanceDetails
3 panels
R-numbers: R39
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Griscelli syndrome, type 2 607624 AR
R-numbers: R236
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
GS2, GRISCELLI SYNDROME, TYPE 2, Griscelli syndrome
R-numbers: R15
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Griscelli syndrome, type 2 607624, Partial albinism, fever, HSM, HLH, cytopenias, Diseases of Immune Dysregulation