{{Rsnum
|rsid=121912511
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=KCNH2
|position=150974825
|Gene_s=KCNH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152427
|rsnum=121912511
|variant=0015
}}{{ClinVar
|rsid=121912511
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=150671913
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNH2:3757
|GENE_NAME=KCNH2
|GENE_ID=3757
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.150671913T>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=152427.0015
|CLNSIG=5
|CLNCUI=C1835325
|CLNDBN=Long QT syndrome 2; not provided
|Disease=Long QT syndrome 2; not provided
|CLNACC=RCV000015515.24; RCV000058063.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C3150943:613688:101016
}}{{PMID Auto
|PMID=12354768
|Title=A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.
}}

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}

{{PMID Auto
|PMID=16922724
|Title=Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
}}

{{PMID Auto
|PMID=21661061
|Title=An NMR study of the N-terminal domain of wild-type hERG and a T65P trafficking deficient hERG mutant.
}}