Canonical Allele Identifier: PA2826977571
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 856240
ClinVar RCV Id: RCV001061654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Ser110Ala
CA378920855
NM_001318054.2:c.328T>G