Canonical Allele Identifier: PA891866191
Gene: TOP2B HGNC NCBI

Linked Data

ClinVar Variation Id: 265791
ClinVar RCV Id: RCV000256202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317629.1:p.His63Tyr
CA10588830
NM_001330700.2:c.187C>T