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Highlights:
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- The GPCR NaVa database integrates data on natural variants in human GPCRs from online databases, the scientific literature, and patents.
- Where available, variants contain information on their location in the DNA (and protein sequence), the involved nucleotides (and amino acids), the average frequency of each allele, reported disease associations, and references to public databases and the scientific literature.
- The GPCR NaVa database aims to facilitate studies into pharmacogenetics, genotype-phenotype, and structure-function relationships of GPCRs.
- The GPCR NaVa database is interlinked with the family-specific GPCRDB resource.
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