Allele Registry

Canonical Allele Identifier: PA150638

Gene: RAB3GAP1 HGNC NCBI

ClinVar RCV:

RCV000087135

ClinVar Variation:

100771

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165906.1:p.Thr18Pro	CA150637 NM_001172435.2:c.52A>C