Canonical Allele Identifier: PA2580532828
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2134374
ClinVar RCV Id: RCV003044909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Arg73His
CA378924593
NM_176795.5:c.218G>A