Allele Registry

Canonical Allele Identifier: PA2826561547

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013152

RCV000164988

RCV000417682

RCV000420507

RCV000426429

RCV000427077

RCV000428361

RCV000431193

RCV000432989

RCV000434905

RCV000437100

RCV000437706

RCV000439021

RCV000443570

RCV000443589

RCV000696673

RCV001221969

RCV002422533

ClinVar Variation:

12358

574679

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Val233Leu	CA000430 NM_001276696.3:c.697G>T CA397837009 NM_001276696.3:c.697G>C