Allele Registry

Canonical Allele Identifier: PA2579934498

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.469550727

Score 1.6911697792

Score -1.2274463506

Score 0.2197344

Score 1.2062020436

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000422121

RCV000422786

RCV000424190

RCV000432351

RCV000433925

RCV000434574

RCV000440467

RCV000441020

RCV000443933

RCV001805037

RCV002508212

RCV002524696

RCV003470375

RCV004022213

ClinVar Variation:

376597

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Phe270Cys	CA16603019 NM_000546.6:c.809T>G