{{Rsnum
|rsid=199476147
|Chromosome=9
|position=35689239
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AAG)
|geno3=(AAG;AAG)
|Gene=TPM2
|Gene_s=TPM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=9
|CLNACC=RCV000013282.22
|CLNALLE=1
|CLNDBN=Cap myopathy 2
|CLNHGVS=NC_000009.11:g.35689236_35689238delCTT
|CLNORIGIN=32
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=190990.0007
|Disease=Cap myopathy 2
|FwdREF=AAG
|GENEINFO=TPM2:7169
|GENE_ID=7169
|GENE_NAME=TPM2
|REF=GCTT
|RSPOS=35689235
|Reversed=1
|SAO=3
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=199476147
|CLNDSDB=MedGen
|CLNDSDBID=CN178537
}}{{PMID Auto
|PMID=19047562
|Title=New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.
}}