Allele Registry

Canonical Allele Identifier: PA658805579

Gene: RAB3GAP1 HGNC NCBI

ClinVar RCV:

RCV000087136

ClinVar Variation:

100772

HGVS (amino-acid)	Matching Registered Transcripts
NP_036365.1:p.Glu24Val	CA150639 NM_012233.3:c.71A>T