Allele Registry

Canonical Allele Identifier: PA107313

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.0911439781

Score 1.4693132837

Score 0.9765200204

Score 0.23555926

Score 0.511078044

Score 0.448634147

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000115732

RCV000200601

RCV000420460

RCV000420651

RCV000422171

RCV000425220

RCV000425854

RCV000430670

RCV000432406

RCV000433924

RCV000435258

RCV000435287

RCV000438314

RCV000444325

RCV000444475

RCV000445147

RCV000492245

RCV000785536

RCV001808343

ClinVar Variation:

127820

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr234Cys	CA000337 NM_000546.6:c.701A>G