Allele Registry

Canonical Allele Identifier: PA2573070697

Gene: TOP2B HGNC NCBI

ClinVar Allele:

1310230

ClinVar RCV:

RCV001775185

ClinVar Variation:

1319982

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317629.1:p.Glu593del	CA2497030038 NM_001330700.2:c.1776_1778del