Allele Registry

Canonical Allele Identifier: PA106641

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.9409324192

Score -1.379240877

Score -0.3786729015

Score -1.172650407

Score -1.666967192

Score 0.2073973703

Score -1.862394142

Score -2.571817302

Score -1.379079715

Score -1.818810162

Linked Data - NCBI & NCI

ClinVar Allele:

181010

ClinVar RCV:

RCV000161065

RCV000810785

RCV002288703

ClinVar Variation:

182963

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg175Leu	CA000252 NM_000546.6:c.524G>T