Allele Registry

Canonical Allele Identifier: PA358288

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.1559467452

Score 0.478831472

Score 0.467671904

Score -1.191916049

Score 0.730753102

Score 1.6750800846

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000204217

RCV000418073

RCV000423238

RCV000424345

RCV000424462

RCV000425587

RCV000430896

RCV000432845

RCV000433328

RCV000433956

RCV000435222

RCV000440475

RCV000441597

RCV000445176

RCV000445265

RCV000492197

RCV004020511

ClinVar Variation:

219759

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr234Asp	CA348450 NM_000546.6:c.700T>G