{{Rsnum
|rsid=137853287
|Chromosome=13
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=ATP7B
|position=51958367
|Gene_s=ATP7B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TG
|CHROM=13
|CLNALLE=1
|CLNDBN=Wilson's disease
|CLNDSDB=OMIM
|CLNDSDBID=277900
|CLNHGVS=NC_000013.10:g.52532503_52532504insG
|CLNSIG=5
|Disease=Wilson's disease
|FwdALT=C
|GENEINFO=ATP7B:540
|GENE_ID=540
|GENE_NAME=ATP7B
|REF=T
|RSPOS=52532497
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;NSF;REF;INT;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050268081201000002110200
|WGT=1
|dbSNPBuildID=133
|rsid=137853287
}}{{PMID Auto
|PMID=9199563
|Title=Haplotype and mutation analysis in Japanese patients with Wilson disease.
|OA=1
}}

{{PMID Auto
|PMID=9504786
|Title=Early and severe neurological features in a Wilson disease patient compound heterozygous for two frameshift mutations.
}}

{{PMID Auto
|PMID=12955875
|Title=Diagnosis and phenotypic classification of Wilson disease.
}}

{{PMID Auto
|PMID=16791614
|Title=Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing.
}}

{{PMID Auto
|PMID=19118915
|Title=Genotype-phenotype correlation in Italian children with Wilson's disease.
}}