Allele Registry

Canonical Allele Identifier: PA296067

Gene: HRAS HGNC NCBI

MaveDb:

Score -0.0902704632

Score 0.004439759

Score 0.1239813337

Score 0.0088265701

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