Canonical Allele Identifier: PA296071
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 180853
ClinVar RCV Id: RCV000157924 RCV001219043
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Met182Val
CA296070
NM_005343.4:c.544A>G