Allele Registry

Canonical Allele Identifier: PA2579935313

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.668963053

Score 1.0132204504

Score 0.156537182

Score 1.5963203037

Score -1.292837231

Score 0.457024043

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419021

RCV000419523

RCV000419702

RCV000421037

RCV000423767

RCV000424584

RCV000426310

RCV000427847

RCV000429130

RCV000429300

RCV000432093

RCV000434035

RCV000434427

RCV000437403

RCV000438068

RCV000438679

RCV000438838

RCV000439357

RCV000443812

RCV000570507

RCV001313857

RCV001575028

RCV004022254

ClinVar Variation:

376688

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr220Asn	CA16603101 NM_000546.6:c.658T>A