Canonical Allele Identifier: PA916071755
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 179260
ClinVar RCV Id: RCV000156047

Amino-acid Alleles

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