Allele Registry

Canonical Allele Identifier: PA645475150

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000421560

RCV000431895

RCV002230756

ClinVar Variation:

375961

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly12Arg	CA16602439 NM_005343.4:c.34G>C