Canonical Allele Identifier: PA916022169
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 409951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ser27Thr
CA5779320
NM_001318054.2:c.79T>A