Allele Registry

Canonical Allele Identifier: PA106619

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.0292788333

Score 0.443261908

Score 1.7301902119

Score 0.9680236083

Score -0.123841699

Score 0.259746395

Score 0.536665221

Score 0.300002032

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419625

RCV000420706

RCV000420923

RCV000421238

RCV000421436

RCV000424235

RCV000425355

RCV000426938

RCV000428548

RCV000430584

RCV000430740

RCV000430935

RCV000432105

RCV000432831

RCV000436078

RCV000436759

RCV000437498

RCV000438570

RCV000441260

RCV000443278

RCV000444080

RCV000444111

RCV000459914

RCV000573315

RCV000785486

RCV001584115

RCV002289532

ClinVar Variation:

376649

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg175Gly	CA16603066 NM_000546.6:c.523C>G