Canonical Allele Identifier: PA206631
Gene: RAB3GAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211978
ClinVar RCV Id: RCV000193269 RCV000224002 RCV000280127 RCV001849339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036365.1:p.Arg336Cys
CA206629
NM_012233.3:c.1006C>T