Canonical Allele Identifier: PA2829600867
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2061405
ClinVar RCV Id: RCV002939038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Met72Thr
CA378924599
NM_005343.4:c.215T>C