Allele Registry

Canonical Allele Identifier: PA106599

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.3599730675

Score -0.597958145

Score 0.9044447027

Score 0.202604818

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000130708

RCV000227859

RCV000255654

RCV000496787

RCV001257522

RCV003461996

RCV003492603

ClinVar Variation:

141963

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg158His	CA000227 NM_000546.6:c.473G>A