Allele Registry

Canonical Allele Identifier: PA2579934228

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.5688106213

Score 0.3700450283

Score 0.508418168

Score 0.6920650184

Score 0.186815948

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418023

RCV000423448

RCV000423739

RCV000423933

RCV000425366

RCV000428734

RCV000428952

RCV000431165

RCV000433592

RCV000433708

RCV000436148

RCV000436528

RCV000438568

RCV000440980

RCV000442077

RCV000444610

RCV000444685

RCV000492483

RCV000633356

ClinVar Variation:

376657

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg280Lys	CA16603072 NM_000546.6:c.839G>A