Allele Registry

Canonical Allele Identifier: PA2579935960

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.787794743

Score -0.017741621

Score -1.4011943086

Score 1.0421076304

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420510

RCV000421224

RCV000421433

RCV000422328

RCV000426919

RCV000427172

RCV000427925

RCV000428125

RCV000431234

RCV000432547

RCV000433456

RCV000434884

RCV000437164

RCV000438275

RCV000439058

RCV000441519

RCV000443703

RCV000444604

RCV000444694

RCV001023982

RCV001861483

ClinVar Variation:

376611

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.His179Pro	CA16603032 NM_000546.6:c.536A>C