Canonical Allele Identifier: PA645494485
Gene: RAB3GAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036365.1:p.Pro423Arg
CA1884799
NM_012233.3:c.1268C>G