Allele Registry

Canonical Allele Identifier: PA337262

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.1113191867

Score -0.489938737

Score 0.5131875362

Score -0.3316245768

Linked Data - NCBI & NCI

ClinVar Allele:

213402

ClinVar RCV:

RCV000197507

RCV000420405

RCV000420607

RCV000421753

RCV000422366

RCV000423507

RCV000425663

RCV000426240

RCV000427801

RCV000430716

RCV000430953

RCV000431571

RCV000433115

RCV000433745

RCV000436943

RCV000437594

RCV000438784

RCV000441651

RCV000442723

RCV000443241

RCV000443320

RCV003165469

ClinVar Variation:

216465

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Thr125Lys	CA337257 NM_000546.6:c.374C>A