Canonical Allele Identifier: PA2829601129
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1692890
ClinVar RCV Id: RCV002258705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Arg161Gly
CA378921170
NM_005343.4:c.481C>G