Allele Registry

Canonical Allele Identifier: PA2826599599

Gene: TOP3B HGNC NCBI

ClinVar RCV:

RCV004180510

ClinVar Variation:

2338671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269042.1:p.Val764Met	CA410834571 NM_001282113.2:c.2290G>A