Allele Registry

Canonical Allele Identifier: PA2579935193

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.286599127

Score 1.6954045392

Score 0.20809237

Score 0.262115381

Score -0.9894306905

Score 0.4644948439

Score 0.535561693

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418805

RCV000421362

RCV000423748

RCV000425382

RCV000426057

RCV000426513

RCV000432031

RCV000433704

RCV000434459

RCV000436060

RCV000441006

RCV000442909

RCV000443654

RCV000492366

RCV000633372

RCV001257520

RCV002289524

RCV003168616

RCV003332172

RCV003476007

ClinVar Variation:

376600

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly244Ser	CA16603022 NM_000546.6:c.730G>A