Allele Registry

Canonical Allele Identifier: PA2826559923

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000418001

RCV000419267

RCV000420351

RCV000424520

RCV000425133

RCV000425485

RCV000430145

RCV000431028

RCV000432729

RCV000435229

RCV000437599

RCV000438254

RCV000443153

ClinVar Variation:

376602

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Gly205Arg	CA16603024 NM_001276695.3:c.613G>C