Canonical Allele Identifier: PA176354
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40435
ClinVar RCV Id: RCV000150834 RCV000150835
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala59Thr
CA176353
NM_005343.4:c.175G>A