Varaico: Literature-Extracted Genetic Variants

Gene:PROKR2
Variant:p.V255I
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PROKR2

NM_144773.4:p.V255I

Associated Papers

Additional mutation in PROKR2 and phenotypic differences in a Kallmann syndrome/normosmic congenital hypogonadotropic hypogonadism family carrying FGFR1 missense mutation.

Ichioka K et al.

Bmj Case Reports, 2024

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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."