Canonical Allele Identifier: PA154832
Gene: RAB3GAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 130063
ClinVar RCV Id: RCV000118090 RCV000346473 RCV000878614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036365.1:p.Tyr442Cys
CA154830
NM_012233.3:c.1325A>G