Allele Registry

Canonical Allele Identifier: PA2827515349

Gene: TOP3B HGNC NCBI

ClinVar RCV:

RCV004201545

ClinVar Variation:

2362505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336780.1:p.Gly249Ser	CA10125725 NM_001349851.2:c.745G>A