Canonical Allele Identifier: PA2829601172
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1334241
ClinVar RCV Id: RCV001813656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro174His
CA378921056
NM_005343.4:c.521C>A