Allele Registry

Canonical Allele Identifier: PA2579936817

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.661034578

Score -1.7548420728

Score 1.3666572351

Score -0.258826379

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000536061

RCV000565366

RCV000759374

RCV002289731

RCV003459202

ClinVar Variation:

458543

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Leu130Val	CA287488714 NM_000546.6:c.388C>G