Allele Registry

Canonical Allele Identifier: PA2826559912

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363457

ClinVar RCV:

RCV000417879

RCV000418512

RCV000424746

RCV000425032

RCV000427153

RCV000433671

RCV000435022

RCV000435743

RCV000438269

RCV000442305

RCV000442449

RCV000688366

RCV000785473

RCV002379285

ClinVar Variation:

376578

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Cys203Phe	CA501203 NM_001276695.3:c.608G>T CA645588597 NM_001276695.3:c.608_609delinsTT