Allele Registry

Canonical Allele Identifier: PA2826567558

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419110

RCV000421308

RCV000421511

RCV000426176

RCV000427234

RCV000428935

RCV000429960

RCV000432174

RCV000433559

RCV000434654

RCV000438516

RCV000439628

RCV000439864

RCV000442747

RCV000443562

RCV000556558

ClinVar Variation:

376590

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Glu247Gly	CA16603012 NM_001276761.3:c.740A>G