Allele Registry

Canonical Allele Identifier: PA2826977520

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV001494759

RCV002330854

ClinVar Variation:

462153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Arg41Lys	CA5779309 NM_001318054.2:c.122G>A