{{Rsnum
|rsid=104895295
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MVK
|position=109574881
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MMAB,MVK
}}{{omim
|id=251170
|rsnum=104895295
|variant=0003
}}
{{omim
|id=260920
|rsnum=104895295
}}{{ClinVar
|rsid=104895295
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=110012686
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MVK:4598; MMAB:326625
|GENE_NAME=MVK; MMAB
|GENE_ID=4598; 326625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.110012686A>C
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=251170.0003; 73
|CLNSIG=5
|CLNCUI=C0398691; C1959626
|CLNDBN=Hyperimmunoglobulin D with periodic fever; Mevalonic aciduria
|Disease=Hyperimmunoglobulin D with periodic fever; Mevalonic aciduria
|CLNACC=RCV000012707.14; RCV000012708.14
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0398691:260920:343:234538002; C1959626:610377:29
}}{{PMID Auto
|PMID=11313768
|Title=Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome.
}}

{{PMID Auto
|PMID=11313769
|Title=Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome.
}}