Allele Registry

Canonical Allele Identifier: PA2579934636

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.520020342

Score -0.80393489

Score 0.628703083

Score -1.596039669

Linked Data - NCBI & NCI

ClinVar Allele:

363459

ClinVar RCV:

RCV000420256

RCV000420917

RCV000421654

RCV000422298

RCV000430938

RCV000431682

RCV000432344

RCV000432990

RCV000438862

RCV000441640

RCV000442778

RCV003621530

ClinVar Variation:

376580

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys242Trp	CA16603005 NM_000546.6:c.726C>G