Allele Registry

Canonical Allele Identifier: PA645435695

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376579

ClinVar RCV Id: RCV000419559 RCV000423712 RCV000424356 RCV000430244 RCV000429187 RCV000431566 RCV000434352 RCV000439881 RCV000441578 RCV000440943 RCV000442629 RCV000662594 RCV001026200 RCV001325155

ClinVar Variation Id: 647334

ClinVar RCV Id: RCV000801823 RCV004028076

ClinVar Variation Id: 2124706

ClinVar RCV Id: RCV003039749

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.Cys242Ser	CA001776 NM_001126114.3:c.725G>C CA16603004 NM_001126114.3:c.724T>A CA2580094896 NM_001126114.3:c.725_726delinsCA