Allele Registry

Canonical Allele Identifier: PA2579936187

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.8709878277

Score -0.0391703737

Score 0.4140515673

Score -0.900088892

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420222

RCV000421293

RCV000422381

RCV000423439

RCV000426285

RCV000427300

RCV000428053

RCV000428730

RCV000432614

RCV000433715

RCV000438265

RCV000438983

RCV000440037

RCV000440518

RCV000442618

RCV000443403

RCV000444401

RCV000633371

RCV000785256

ClinVar Variation:

376639

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro151His	CA16603056 NM_000546.6:c.452C>A CA645589093 NM_000546.6:c.452_453delinsAT