Varaico: Literature-Extracted Genetic Variants

Gene:NEXN
Variant:p.R397W
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NEXN

NM_144573.4:p.R397W

Associated Papers

Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth.

Sahlin E et al.

Plos One, 2019

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."