Allele Registry

Canonical Allele Identifier: PA151494

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.5298945279

Score -0.1282095396

Score -0.5503470875

Linked Data - NCBI & NCI

ClinVar Allele:

133262

ClinVar RCV:

RCV000115716

RCV000409540

RCV000679367

RCV001082818

RCV001796963

RCV003891612

ClinVar Variation:

127805

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ala83Val	CA000083 NM_000546.6:c.248C>T