Allele Registry

Canonical Allele Identifier: PA2827515090

Gene: TOP3B HGNC NCBI

ClinVar RCV:

RCV004201545

ClinVar Variation:

2362505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336774.1:p.Gly385Ser	CA10125725 NM_001349845.2:c.1153G>A