Allele Registry

Canonical Allele Identifier: PA2579935271

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.0724019305

Score -0.192124294

Score 0.455404087

Score 1.1445427781

Score 0.9213923463

Score -0.807006741

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418366

RCV000419457

RCV000420564

RCV000422775

RCV000423557

RCV000424609

RCV000425684

RCV000426866

RCV000429686

RCV000432077

RCV000434790

RCV000434877

RCV000435947

RCV000437125

RCV000440449

RCV000441702

RCV000441931

RCV000441961

RCV000443160

RCV001045859

RCV002374627

RCV004022242

ClinVar Variation:

376665

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ser241Ala	CA16603080 NM_000546.6:c.721T>G