Allele Registry

Canonical Allele Identifier: PA915954774

Gene: TOP2A HGNC NCBI

ClinVar RCV:

RCV000890315

RCV003957933

ClinVar Variation:

717511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001058.2:p.Lys893Arg	CA8543329 NM_001067.4:c.2678A>G