Allele Registry

Canonical Allele Identifier: PA2826562513

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418465

RCV000419917

RCV000420625

RCV000421324

RCV000424417

RCV000426479

RCV000427170

RCV000429590

RCV000430194

RCV000431582

RCV000435565

RCV000436708

RCV000438255

RCV000439157

RCV000439619

RCV000439812

RCV000445156

RCV000568150

RCV000706131

RCV000785300

RCV003476010

RCV004022240

ClinVar Variation:

376658

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Arg121Gly	CA16603073 NM_001276697.3:c.361A>G