Allele Registry

Canonical Allele Identifier: PA2579936186

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.9611559374

Score 0.9411817183

Score -1.69264906

Score -0.318906261

Linked Data - NCBI & NCI

ClinVar Allele:

363519

ClinVar RCV:

RCV000418846

RCV000419325

RCV000419958

RCV000421526

RCV000423715

RCV000424514

RCV000425600

RCV000430235

RCV000431352

RCV000434196

RCV000435439

RCV000435893

RCV000436541

RCV000439174

RCV000440477

RCV000441608

RCV000443101

RCV000633382

RCV003168617

RCV004022232

ClinVar Variation:

376640

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro151Arg	CA16603057 NM_000546.6:c.452C>G