Canonical Allele Identifier: PA2826977562
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1369069
ClinVar RCV Id: RCV001874567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Cys105Tyr
CA378920919
NM_001318054.2:c.314G>A