Allele Registry

Canonical Allele Identifier: PA2826977478

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000533738

RCV002257459

ClinVar Variation:

180852

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Ala17Pro	CA296068 NM_001318054.2:c.49G>C