Canonical Allele Identifier: PA658819697
Gene: TOP3A HGNC NCBI

Linked Data

ClinVar Variation Id: 446285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004609.1:p.Met100Val
CA8430293
NM_004618.5:c.298A>G