Allele Registry

Canonical Allele Identifier: PA167860

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.1055108073

Score 0.542016636

Score -0.739172974

Score -0.636890548

Score -0.695047204

Score 0.9605549718

Score -0.0030684225

Score 0.449213735

Score 0.610301825

Score -0.89649447

Score 0.753765542

Score -0.693918318

Score -0.236741394

Score 0.499489974

Score -0.033514152

Score -0.010954139

Score -0.338219422

Score 0.158969421

Score -0.907145368

Score 0.832604708

Score 0.619706805

Score 0.319246953

Score 0.667612602

Score -0.129863331

Score -0.506603485

Score 0.421352529

Score -0.044213961

Score 0.031651904

Linked Data - NCBI & NCI

ClinVar Allele:

151955

ClinVar RCV:

RCV000131246

RCV000419499

RCV000419850

RCV000420497

RCV000421647

RCV000421887

RCV000427275

RCV000429077

RCV000429319

RCV000430131

RCV000431473

RCV000437502

RCV000438874

RCV000439985

RCV000440358

RCV000445113

RCV000724753

RCV001857457

RCV002288647

ClinVar Variation:

142241

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg249Lys	CA000391 NM_000546.6:c.746G>A