Canonical Allele Identifier: PA2829601107
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 964643
ClinVar RCV Id: RCV001238905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala155Val
CA378921211
NM_005343.4:c.464C>T