Allele Registry

Canonical Allele Identifier: PA2825397077

Gene: TOP2B HGNC NCBI

ClinVar RCV:

RCV000256202

ClinVar Variation:

265791

HGVS (amino-acid)	Matching Registered Transcripts
NP_001059.2:p.His58Tyr	CA10588830 NM_001068.3:c.172C>T