Canonical Allele Identifier: PA2742019190
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1810343
ClinVar RCV Id: RCV003238902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Ala59Gly
CA378924683
NM_176795.5:c.176C>G