ID   CHDIi017-A
AC   CVCL_VC88
SY   #17c1; CHDI-90002165
DR   BioSamples; SAMEA4675645
DR   EBiSC; CHDIi017-A
DR   ECACC; 66541172
DR   hPSCreg; CHDIi017-A
DR   Wikidata; Q54811779
CC   From: CHDI Foundation; New York; USA.
CC   Sequence variation: Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[45] (c.52CAG(45)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (EBiSC).
CC   Derived from sampling site: Cell type=Fibroblast.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Male
AG   45-49Y
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 16-12-21; Version: 7
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