Allele Registry

Canonical Allele Identifier: PA2826567555

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417903

RCV000420631

RCV000423140

RCV000424403

RCV000425922

RCV000430027

RCV000430739

RCV000432539

RCV000435554

RCV000436172

RCV000438282

RCV000440264

RCV000443104

RCV000443133

RCV000443946

RCV003621531

ClinVar Variation:

376592

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Glu247Val	CA16603014 NM_001276761.3:c.740A>T