Canonical Allele Identifier: PA2829600821
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1810343
ClinVar RCV Id: RCV003238902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ala59Gly
CA378924683
NM_005343.4:c.176C>G