Canonical Allele Identifier: PA2829601116
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 3015521
ClinVar RCV Id: RCV003871128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr158Lys
CA378921186
NM_005343.4:c.473C>A