Allele Registry

Canonical Allele Identifier: PA2826562069

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417872

RCV000418906

RCV000423862

RCV000424176

RCV000426347

RCV000428105

RCV000428760

RCV000430958

RCV000433698

RCV000435531

RCV000436591

RCV000437249

RCV000438368

RCV000440868

RCV000441249

RCV000443239

ClinVar Variation:

376683

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Tyr46Ser	CA16603097 NM_001276697.3:c.137A>C