{{Rsnum
|rsid=193922673
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PKP2
|position=32821473
|Gene_s=PKP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922673
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=32974407
|CHROM=12
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.32974407C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy
|Disease=Arrhythmogenic right ventricular cardiomyopathy
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000030361.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1131:C0349788:253528005:281170005
|GENEINFO=PKP2:5318
|GENE_ID=5318
|GENE_NAME=PKP2
}}{{PMID Auto
|PMID=16567567
|Title=Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy.
}}

{{PMID Auto
|PMID=18382419
|Title=Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
|OA=1
}}

{{PMID Auto
|PMID=20031616
|Title=Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study.
}}