Allele Registry

Canonical Allele Identifier: PA2579935335

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.4711605786

Score -0.5572392497

Score 0.351055988

Score 0.128279555

Score 0.244862351

Score 1.0312808494

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420217

RCV000420881

RCV000423272

RCV000429840

RCV000430889

RCV000433950

RCV000435696

RCV000440493

RCV000441630

RCV000785347

RCV001025280

RCV003509529

ClinVar Variation:

376660

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ser215Ile	CA16603075 NM_000546.6:c.644G>T CA3047147247 NM_000546.6:c.644_645delinsTA