Allele Registry

Canonical Allele Identifier: PA2579936489

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.9293481186

Score -0.4887307457

Score 0.84238474

Score -0.242534082

Linked Data - NCBI & NCI

ClinVar Allele:

363438

ClinVar RCV:

RCV000417503

RCV000418582

RCV000425788

RCV000426876

RCV000427781

RCV000428180

RCV000434318

RCV000435797

RCV000436440

RCV000436707

RCV000438861

RCV000444308

RCV000444605

RCV000492398

RCV001203469

RCV004022199

ClinVar Variation:

376559

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys135Phe	CA16602985 NM_000546.6:c.404G>T