Allele Registry

Canonical Allele Identifier: PA916071829

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000533738

RCV002257459

ClinVar Variation:

180852

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Arg123Pro	CA296068 NM_176795.5:c.368G>C