Allele Registry

Canonical Allele Identifier: PA2579936158

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.0212856504

Score -1.982537508

Score 0.6113738436

Score -1.0202973729

Linked Data - NCBI & NCI

ClinVar Allele:

410274

ClinVar RCV:

RCV000481578

RCV000561574

RCV000795252

RCV002289645

ClinVar Variation:

422563

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro153Ser	CA16620631 NM_000546.6:c.457C>T