Canonical Allele Identifier: PA2573070216
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1321132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Val73Met
CA378921257
NM_001318054.2:c.217G>A