Allele Registry

Canonical Allele Identifier: PA2826562066

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000419308

RCV000420368

RCV000421826

RCV000422887

RCV000424493

RCV000426781

RCV000427755

RCV000431739

RCV000431958

RCV000432726

RCV000437451

RCV000437587

RCV000439923

RCV000440094

RCV000443622

RCV000443753

RCV000775886

RCV000819983

RCV004022252

ClinVar Variation:

376685

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Tyr46His	CA16603099 NM_001276697.3:c.136T>C