Canonical Allele Identifier: PA2829600916
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 940277
ClinVar RCV Id: RCV001209828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Asp92Asn
CA378924350
NM_005343.4:c.274G>A