Canonical Allele Identifier: PA231432
Gene: RAB3GAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 130066
ClinVar RCV Id: RCV000118093 RCV000267107
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Amino-acid Alleles

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