Allele Registry

Canonical Allele Identifier: PA2826564118

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363551

ClinVar RCV:

RCV000418104

RCV000418474

RCV000419558

RCV000423283

RCV000424832

RCV000429571

RCV000429825

RCV000434860

RCV000436131

RCV000439819

RCV000440944

RCV002356519

ClinVar Variation:

376672

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263628.1:p.Val57Glu	CA16603086 NM_001276699.3:c.170T>A