Allele Registry

Canonical Allele Identifier: PA2826564141

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363568

ClinVar RCV:

RCV000417982

RCV000418575

RCV000418779

RCV000422783

RCV000424311

RCV000425315

RCV000426793

RCV000427506

RCV000428144

RCV000430837

RCV000431034

RCV000433449

RCV000434918

RCV000436457

RCV000437034

RCV000440413

RCV000441127

RCV000444073

RCV000444915

RCV001851023

RCV004022255

ClinVar Variation:

376689

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263628.1:p.Tyr61Asp	CA16603102 NM_001276699.3:c.181T>G