Canonical Allele Identifier: PA2829601124
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1938886
ClinVar RCV Id: RCV002646576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Val160Gly
CA378921172
NM_005343.4:c.479T>G