Allele Registry

Canonical Allele Identifier: PA2580299535

Gene: TOP3B HGNC NCBI

ClinVar Allele:

2346074

ClinVar RCV:

RCV004201545

ClinVar Variation:

2362505

HGVS (amino-acid)	Matching Registered Transcripts
NP_003926.1:p.Gly385Ser	CA10125725 NM_003935.5:c.1153G>A