RAB1A

RAB1A, member RAS oncogene family
OMIM: 179508
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
RAB1A-related neurodevelopmental disorder with speech and motor delay and spasticity