Allele Registry

Canonical Allele Identifier: PA2579935844

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.993050203

Score 0.7551777913

Score 0.3160465527

Score -0.4224215405

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000580691

RCV000986052

RCV002289855

RCV002509455

RCV003767274

ClinVar Variation:

490174

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Thr170Arg	CA287488567 NM_000546.6:c.509C>G