Allele Registry

Canonical Allele Identifier: PA2579953097

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.6605257763

Score -0.8200333274

Score 0.2329885046

Linked Data - NCBI & NCI

ClinVar Allele:

420661

ClinVar RCV:

RCV000492393

RCV000505579

RCV002274041

RCV002289672

RCV003509552

ClinVar Variation:

428887

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val157Ala	CA397842041 NM_000546.6:c.470T>C