Allele Registry

Canonical Allele Identifier: PA2825617786

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363489

ClinVar RCV:

RCV000419821

RCV000420116

RCV000421694

RCV000423899

RCV000424030

RCV000425288

RCV000426383

RCV000430072

RCV000430612

RCV000431709

RCV000431956

RCV000436443

RCV000436622

RCV000437679

RCV000440707

RCV000441771

RCV000443866

RCV000444860

RCV000444992

RCV001851020

RCV002348144

RCV002465649

RCV003335320

RCV003470376

ClinVar Variation:

376610

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119590.1:p.His140Asp	CA16603031 NM_001126118.1:c.418C>G