Allele Registry

Canonical Allele Identifier: PA2825397390

Gene: TOP2B HGNC NCBI

ClinVar Allele:

1310230

ClinVar RCV:

RCV001775185

ClinVar Variation:

1319982

HGVS (amino-acid)	Matching Registered Transcripts
NP_001059.2:p.Glu588del	CA2497030038 NM_001068.3:c.1761_1763del