Allele Registry

Canonical Allele Identifier: PA2826565598

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376661

ClinVar RCV Id: RCV000421044 RCV000422178 RCV000425174 RCV000431745 RCV000432876 RCV000437603 RCV000439391 RCV000442610 RCV000442691 RCV000465501 RCV000662560 RCV000785463 RCV002289537

ClinVar Variation Id: 428895

ClinVar RCV Id: RCV000492567 RCV004023282 RCV002523445

ClinVar Variation Id: 2020649

ClinVar RCV Id: RCV002857438

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263689.1:p.Ser176Arg	CA16603076 NM_001276760.3:c.528T>G CA397839990 NM_001276760.3:c.528T>A CA397840019 NM_001276760.3:c.526A>C