Canonical Allele Identifier: PA2829600798
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2767695
ClinVar RCV Id: RCV003515956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Leu53Trp
CA378924721
NM_005343.4:c.158T>G