Allele Registry

Canonical Allele Identifier: PA2579934323

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.0044960307

Score 0.16748279

Score 0.9920200656

Score -0.118197754

Score 1.5887217663

Linked Data - NCBI & NCI

ClinVar Allele:

363553

ClinVar RCV:

RCV000418237

RCV000418736

RCV000419355

RCV000423526

RCV000428932

RCV000429450

RCV000430114

RCV000435470

RCV000436116

RCV000440120

RCV000440773

RCV001255677

RCV001344689

RCV002429349

RCV004022248

ClinVar Variation:

376674

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val274Phe	CA16603088 NM_000546.6:c.820G>T