ID   GM23385
AC   CVCL_BV62
DR   Coriell; GM23385
DR   Wikidata; Q54853036
CC   Sequence variation: Mutation; HGNC; HGNC:6251; KCNH2; Unexplicit; Large deletion; Zygosity=Unspecified (Coriell=GM23385).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C137957; Long QT syndrome 2
DI   ORDO; Orphanet_101016; Romano-Ward syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   56Y
CA   Finite cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 12
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