Canonical Allele Identifier: PA2829600870
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2134374
ClinVar RCV Id: RCV003044909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg73His
CA378924593
NM_005343.4:c.218G>A