Canonical Allele Identifier: PA2829600864
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1060724
ClinVar RCV Id: RCV001370190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Tyr71His
CA378924610
NM_005343.4:c.211T>C