Allele Registry

Canonical Allele Identifier: PA2825610790

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363458

646750

2181300

ClinVar RCV:

RCV000419559

RCV000423712

RCV000424356

RCV000429187

RCV000430244

RCV000431566

RCV000434352

RCV000439881

RCV000440943

RCV000441578

RCV000442629

RCV000662594

RCV000801823

RCV001026200

RCV001325155

RCV003039749

RCV004028076

ClinVar Variation:

376579

647334

2124706

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.Cys110Ser	CA001776 NM_001126115.1:c.329G>C CA16603004 NM_001126115.1:c.328T>A CA2580094896 NM_001126115.1:c.329_330delinsCA