Canonical Allele Identifier: PA2580323461
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2089966
ClinVar RCV Id: RCV003005736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ser189Ter
CA2580083835
NM_005343.4:c.566_568del