Allele Registry

Canonical Allele Identifier: PA2826566007

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000129516

RCV000418257

RCV000418481

RCV000423760

RCV000423959

RCV000425885

RCV000426980

RCV000428043

RCV000429146

RCV000431187

RCV000433596

RCV000434395

RCV000435472

RCV000436592

RCV000436807

RCV000438583

RCV000441016

RCV000442068

RCV000442813

RCV000633367

RCV002288626

RCV003237737

ClinVar Variation:

141141

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263689.1:p.Asp242Gly	CA000450 NM_001276760.3:c.725A>G CA3047147246 NM_001276760.3:c.725_726delinsGA