Canonical Allele Identifier: PA2829600905
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 935657
ClinVar RCV Id: RCV001204299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Lys88Arg
CA378924406
NM_005343.4:c.263A>G