Allele Registry

This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.

Canonical Allele Identifier: PA231432

Gene: RAB3GAP1 HGNC NCBI

ClinVar RCV:

RCV000118093

RCV000267107

ClinVar Variation:

130066

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165906.1:p.His669Gln	CA231431 NM_001172435.2:c.2007C>A CA348581448 NM_001172435.2:c.2007C>G