Canonical Allele Identifier: PA2829601170
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1024818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro173Ser
CA378921072
NM_005343.4:c.517C>T