Canonical Allele Identifier: PA2826559697
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376686
ClinVar RCV Id: RCV000421137 RCV000419128 RCV000423676 RCV000421350 RCV000426948 RCV000428535 RCV000428939 RCV000430021 RCV000434351 RCV000434446 RCV000438356 RCV000436740 RCV000439865 RCV000439629 RCV000444122 RCV000444873 RCV000462351 RCV000663307 RCV003441853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr166Asp
CA16603100
NM_001276695.3:c.496T>G