vomeronasal type-1 receptor 5; V1r-like receptor 5; hGPCR26 (VN1R5, V1RL5)

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Function

Structure

Compartment

Genetics

Polymorphism

  • allele VN1R5*2 with a truncating mutation in position 46, found with a frequency of about 32%

More general terms

Additional terms

References

Database