Allele Registry

Canonical Allele Identifier: PA916071755

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000156047

ClinVar Variation:

179260

HGVS (amino-acid)	Matching Registered Transcripts
NP_789765.1:p.Ala59Leu	CA273607 NM_176795.5:c.175_176delinsCT