Canonical Allele Identifier: PA2741827352
Gene: TOP2A HGNC NCBI
ClinVar RCV:
RCV004289790
ClinVar Variation:
2517067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001058.2:p.Gly1431Cys
CA399349125
NM_001067.4:c.4291G>T