Allele Registry

Canonical Allele Identifier: PA2579952444

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.7323980175

Score 0.1858345649

Score -0.50778087

Score 0.6177597689

Score -0.001229964

Linked Data - NCBI & NCI

ClinVar Allele:

469122

ClinVar RCV:

RCV000532028

RCV002431551

RCV003409773

RCV004023791

ClinVar Variation:

458567

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys277Phe	CA001518 NM_000546.6:c.830G>T