Allele Registry

Canonical Allele Identifier: PA2826559194

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363511

ClinVar RCV:

RCV000421931

RCV000424730

RCV000433045

RCV000433598

RCV000434970

RCV000442091

RCV000442462

RCV000443054

RCV001041362

RCV004022228

ClinVar Variation:

376632

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Leu72Gln	CA16603051 NM_001276695.3:c.215T>A