Canonical Allele Identifier: PA2826567222
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216469
ClinVar RCV Id: RCV000198628 RCV000492107 RCV004020463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Tyr197His
CA338059
NM_001276761.3:c.589T>C