Allele Registry

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Canonical Allele Identifier: PA2826566470

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473030

ClinVar RCV Id: RCV001969440

ClinVar Variation Id: 1775671

ClinVar RCV Id: RCV002405782

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Trp14Arg	CA397846498 NM_001276761.3:c.40T>C CA397846503 NM_001276761.3:c.40T>A