ID   CHDIi021-A
AC   CVCL_VC92
SY   #21C5
DR   BioSamples; SAMEA1088053
DR   EBiSC; CHDIi021-A
DR   ECACC; 66541156
DR   hPSCreg; CHDIi021-A
DR   Wikidata; Q54811787
CC   From: CHDI Foundation; New York; USA.
CC   Sequence variation: Heterozygous for HTT p.Gln18[44]; has 44 CAG repeats in one of the 2 alleles (hPSCreg).
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens
SX   Male
AG   40-44Y
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 12-03-20; Version: 4
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