Allele Registry

Canonical Allele Identifier: PA2579934201

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.312202549

Score 0.519472413

Score 0.180238365

Score -0.270910307

Score -0.147672924

Score 0.416204486

Score 1.269092904

Score 0.191254801

Score 0.341974639

Score 1.7339534027

Score 0.632741847

Score 0.184509045

Score -0.051826454

Score 0.373299385

Score 0.128800975

Score -1.819235875

Score 1.4690391286

Score -0.175262744

Score 0.393671874

Score 0.24056887

Score 0.022151778

Score -0.358110515

Score 0.673262313

Score 0.314218208

Score -0.162942233

Score 0.211880186

Score 0.161811106

Score 0.035550328

Score 0.316281147

Score 0.416641134

Score 0.438512314

Score 0.435368374

Score 0.157284661

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417824

RCV000417919

RCV000419006

RCV000423005

RCV000423789

RCV000424978

RCV000425389

RCV000426071

RCV000427957

RCV000428608

RCV000432620

RCV000433722

RCV000434763

RCV000435036

RCV000438637

RCV000440221

RCV000441023

RCV000441861

RCV000442220

RCV000492764

RCV000709402

RCV002289536

RCV002502456

ClinVar Variation:

376659

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg282Pro	CA16603074 NM_000546.6:c.845G>C