gene is highly polymorphic and many disease causing mutations are present in
A list of these sequence variants can be found in the supplementary material
to the publication
DeVore and Scott, 2012 (Supplementary Table 2.
Summary of CYP17A1 mutations, their effects, and structural context).
The alleles with these mutations are hitherto not characterized and therefore
no allelic nomenclature has yet been worked out.