Allele Registry

Canonical Allele Identifier: PA916006412

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013145

RCV000013146

RCV000464372

RCV000465003

RCV000579519

RCV000785491

RCV001270276

RCV001562247

RCV003996089

RCV004018617

RCV004022606

ClinVar Variation:

12352

406598

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263628.1:p.Arg90Ser	CA000392 NM_001276699.3:c.270G>T CA16615944 NM_001276699.3:c.270G>C