The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene.

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Jimenez-Cervantes C, Olivares C, Gonzalez P, Morandini R, Ghanem G, Garcia-Borron JC

The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene.

J Invest Dermatol. 2001 Jul;117(1):156-8.

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11442765 [ View in PubMed
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Polypeptides
NameUniProt ID
Melanocyte-stimulating hormone receptorQ01726Details