Allele Registry

Canonical Allele Identifier: PA2826562522

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376587

ClinVar RCV Id: RCV000417671 RCV000420516 RCV000419836 RCV000422083 RCV000422714 RCV000424389 RCV000424902 RCV000430093 RCV000430695 RCV000432322 RCV000431703 RCV000432958 RCV000438151 RCV000439711 RCV000440974 RCV000440370 RCV000443165 RCV000443254 RCV000633352 RCV000785286 RCV002446643

ClinVar Variation Id: 406568

ClinVar RCV Id: RCV000470818 RCV000499361 RCV000658764 RCV000785325 RCV002446795

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Asp122Glu	CA10590135 NM_001276697.3:c.366C>G CA16615937 NM_001276697.3:c.366C>A