Canonical Allele Identifier: PA150653
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 100787
ClinVar RCV Id: RCV000087150 RCV000850507 RCV001807041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.Arg426Cys
CA150652
NM_012414.4:c.1276C>T