Allele Registry

Canonical Allele Identifier: PA166354

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.507728584

Score -0.2799421634

Score 1.0303613673

Score -0.645608308

Score 0.0708454632

Linked Data - NCBI & NCI

ClinVar Allele:

151478

ClinVar RCV:

RCV000130398

RCV000413074

RCV000538977

RCV000763416

RCV001255676

RCV002247507

RCV002288637

RCV003149899

RCV003460927

ClinVar Variation:

141764

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg267Trp	CA000423 NM_000546.6:c.799C>T