Allele Registry

Canonical Allele Identifier: PA2579935198

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.4731090078

Score -0.145371527

Score -0.3208787155

Score 0.148679097

Score 0.7540166439

Score 0.009299794

Linked Data - NCBI & NCI

ClinVar Allele:

363453

ClinVar RCV:

RCV000417498

RCV000418555

RCV000422481

RCV000422719

RCV000425072

RCV000427235

RCV000427531

RCV000428817

RCV000432745

RCV000433862

RCV000433989

RCV000435149

RCV000435343

RCV000439349

RCV000440369

RCV000442469

RCV000444988

RCV000473420

RCV002365459

RCV004022207

ClinVar Variation:

376574

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys238Phe	CA16603000 NM_000546.6:c.713G>T