Varaico: Literature-Extracted Genetic Variants

Gene:PRH2
Variant:p.A9D
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PRH2

NM_001110213.1:p.A9D

Associated Papers

Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficiencies.

Gandrille S et al.

Blood, 1995

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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."