Canonical Allele Identifier: PA2829600869
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2973421
ClinVar RCV Id: RCV003830515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg73Cys
CA216882919
NM_005343.4:c.217C>T