Canonical Allele Identifier: PA2742019206
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2973421
ClinVar RCV Id: RCV003830515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Arg73Cys
CA216882919
NM_176795.5:c.217C>T