Canonical Allele Identifier: PA296063
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 40439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ile93Val
CA296061
NM_176795.5:c.277A>G