Allele Registry

Canonical Allele Identifier: PA296067

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000157922

RCV000471505

RCV000606057

ClinVar Variation:

180851

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Arg123Cys	CA296066 NM_005343.4:c.367C>T