ID   STBCi005-A
AC   CVCL_RB37
SY   SFC833-03-01
DR   BioSamples; SAMEA104129750
DR   EBiSC; STBCi005-A
DR   ECACC; 66540583
DR   hPSCreg; STBCi005-A
DR   Wikidata; Q54956329
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. Cell type=Fibroblast.
DI   NCIt; C26845; Parkinson's disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_RB38 ! STBCi005-B
OI   CVCL_RB39 ! STBCi005-C
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 17-03-22; Version: 9
//