Allele Registry

Canonical Allele Identifier: PA658805576

Gene: RAB3GAP1 HGNC NCBI

ClinVar RCV:

RCV000087135

ClinVar Variation:

100771

HGVS (amino-acid)	Matching Registered Transcripts
NP_036365.1:p.Thr18Pro	CA150637 NM_012233.3:c.52A>C