ID   STBCi005-C
AC   CVCL_RB39
SY   SFC833-03-14
DR   BioSamples; SAMEA104615894
DR   EBiSC; STBCi005-C
DR   ECACC; 66540908
DR   hPSCreg; STBCi005-C
DR   Wikidata; Q54956331
CC   From: StemBANCC; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (EBiSC).
CC   Derived from sampling site: Skin; dermis.
DI   NCIt; C26845; Parkinson's disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_RB37 ! STBCi005-A
OI   CVCL_RB38 ! STBCi005-B
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 16-12-21; Version: 8
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