Canonical Allele Identifier: PA2580136611
Gene: TOP2A HGNC NCBI
ClinVar RCV:
RCV004133955
ClinVar Variation:
2281352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001058.2:p.Arg1435Gly
CA8542925
NM_001067.4:c.4303A>G