Canonical Allele Identifier: PA2826560122
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185722
ClinVar RCV Id: RCV000165199 RCV000254809 RCV000456858 RCV001357202 RCV003474865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Cys238Tyr
CA000438
NM_001276695.3:c.713G>A