Allele Registry

Canonical Allele Identifier: PA169755

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.166905356

Score 0.855815936

Score 0.32241656

Score 0.286476725

Score -2.67510606

Score -3.049722957

Score -0.563791538

Score -2.682788814

Score 0.335990127

Score -1.491785938

Score -0.416842703

Score 0.580028382

Score 0.371254108

Score -3.84994574

Score -5.560322729

Score 0.334209224

Score -0.497536592

Score -1.767329965

Score 0.182896947

Score -0.3675086641

Score -0.310502662

Score -1.06758038

Score 0.472216897

Score 0.449213735

Score -2.427377873

Score 0.944152956

Score -2.37408003

Score -0.091155289

Score 0.518935174

Score 0.3074297872

Score 0.5723096594

Score -0.312202549

Score 0.039060551

Score -4.053809822

Linked Data - NCBI & NCI

ClinVar Allele:

152630

ClinVar RCV:

RCV000132389

RCV000474969

RCV000663318

RCV000679373

ClinVar Variation:

142916

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asn263Asp	CA000419 NM_000546.6:c.787A>G