Canonical Allele Identifier: PA160027
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134514
ClinVar RCV Id: RCV000121201 RCV000813562
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr158Met
CA160026
NM_005343.4:c.473C>T