Canonical Allele Identifier: PA2829601105
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1063343
ClinVar RCV Id: RCV001373169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala155Thr
CA378921219
NM_005343.4:c.463G>A