Canonical Allele Identifier: PA2826977566
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1713318
ClinVar RCV Id: RCV002304250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Val108Met
CA378920877
NM_001318054.2:c.322G>A