Canonical Allele Identifier: PA2829601151
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2821352
ClinVar RCV Id: RCV003628010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gln165Lys
CA378921150
NM_005343.4:c.493C>A