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Items: 2

    • Showing Current items.

    Name/Gene IDDescriptionLocationAliasesMIM
    ID: 7486
    Werner syndrome RecQ like helicase [Homo sapiens (human)]Chromosome 8, NC_000008.11 (31033262..31173761)RECQ3, RECQL2, RECQL3604611
    ID: 2237
    flap structure-specific endonuclease 1 [Homo sapiens (human)]Chromosome 11, NC_000011.10 (61792637..61797244)FEN-1, MF1, RAD2600393
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