Canonical Allele Identifier: PA2579932003
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr158Met
CA160026
NM_001130442.3:c.473C>T