Canonical Allele Identifier: PA2499247991
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1063343
ClinVar RCV Id: RCV001373169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ala76Thr
CA378921219
NM_001318054.2:c.226G>A