Allele Registry

Canonical Allele Identifier: PA2826561882

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000580691

RCV000986052

RCV002289855

RCV002509455

RCV003767274

ClinVar Variation:

490174

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Thr11Arg	CA287488567 NM_001276697.3:c.32C>G