Allele Registry

Canonical Allele Identifier: PA2580136603

Gene: TOP2A HGNC NCBI

ClinVar RCV:

RCV004132709

ClinVar Variation:

2284842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001058.2:p.Glu1230Gly	CA399352436 NM_001067.4:c.3689A>G