Canonical Allele Identifier: PA2825396998
Gene: TOP2A HGNC NCBI
ClinVar RCV:
RCV004468050
ClinVar Variation:
3181183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001058.2:p.Gln1260Arg
CA290526087
NM_001067.4:c.3779A>G