Canonical Allele Identifier: PA2829600772
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1032989
ClinVar RCV Id: RCV001335259 RCV003169563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Val45Asp
CA216882995
NM_005343.4:c.134T>A