Allele Registry

Canonical Allele Identifier: PA2826561913

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363452

622616

ClinVar RCV:

RCV000419497

RCV000419681

RCV000421755

RCV000423671

RCV000425379

RCV000430429

RCV000430876

RCV000431070

RCV000431573

RCV000436082

RCV000436236

RCV000436752

RCV000438958

RCV000441815

RCV000444713

RCV000785469

RCV000785487

RCV001023833

RCV001044520

RCV004022206

ClinVar Variation:

376573

634759

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Cys17Arg	CA16602999 NM_001276697.3:c.49T>C CA913191047 NM_001276697.3:c.49_51delinsCGG