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Results: 4

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    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 80870
    Dyskeratosis, hereditary benign intraepithelial [Homo sapiens (human)]127600
    ID: 3868
    keratin 16, type I [Homo sapiens (human)]Chromosome 17, NC_000017.11 (41609778..41612827, complement)CK16, FNEPPK, K16, K1CPA, NEPPK, PC1, KRT16148067
    ID: 3851
    keratin 4, type II [Homo sapiens (human)]Chromosome 12, NC_000012.12 (52806543..52814116, complement)CK-4, CK4, CYK4, K4, WSN1123940
    ID: 488
    ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 [Homo sapiens (human)]Chromosome 12, NC_000012.12 (110281227..110351093)ATP2B, DAR, DD, SERCA2108740

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