Allele Registry

Canonical Allele Identifier: PA103555

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013442

RCV000485616

RCV002272015

ClinVar Variation:

12608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Glu63Lys	CA122551 NM_001130442.3:c.187G>A