{{Rsnum
|rsid=193922109
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATP7B
|position=51937342
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922109
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=52511478
|CHROM=13
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.52511478G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wilson's disease
|Disease=Wilson's disease
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029377.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1512:C0019202:277900:905:88518009
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
}}{{PMID Auto
|PMID=1789787
|Title=Two-dimensional nuclear magnetic resonance study of brain natriuretic peptide in aqueous solution.
}}

{{PMID Auto
|PMID=8533760
|Title=Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations.
|OA=1
}}

{{PMID Auto
|PMID=9311736
|Title=Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses.
|OA=1
}}

{{PMID Auto
|PMID=11472373
|Title=Haemolytic onset of Wilson disease in a patient with homozygous truncation of ATP7B at Arg1319.
}}

{{PMID Auto
|PMID=16545904
|Title=Different neurological outcome of liver transplantation for Wilson's disease in two homozygotic twins.
}}

{{PMID Auto
|PMID=18034201
|Title=Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneity.
}}