Allele Registry

Canonical Allele Identifier: PA106848

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.153859942

Score 0.1689081634

Score -0.0967101033

Score -2.631680681

Score 0.297665852

Score -2.67245347

Linked Data - NCBI & NCI

ClinVar Allele:

133278

ClinVar RCV:

RCV000115733

RCV000122177

RCV000148915

RCV000590586

RCV000663295

RCV000989714

RCV000991139

RCV001798339

RCV003952552

ClinVar Variation:

127821

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asn235Ser	CA000343 NM_000546.6:c.704A>G