ID   STBCi028-B
AC   CVCL_RB92
SY   SFC018-03-02
DR   BioSamples; SAMEA104493667
DR   EBiSC; STBCi028-B
DR   ECACC; 66540701
DR   hPSCreg; STBCi028-B
DR   Wikidata; Q54956429
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:1388; CACNA1A; Simple; p.Arg582Gln (c.1745G>A) (p.Arg583Gln, c.1748G>A); ClinVar=VCV000008505; Zygosity=Heterozygous (from autologous cell line STBCi028-A).
CC   Discontinued: ECACC; 66540701; true.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C189277; Familial hemiplegic migraine-1
DI   ORDO; Orphanet_569; Familial or sporadic hemiplegic migraine
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_RB91 ! STBCi028-A
OI   CVCL_RB93 ! STBCi028-C
SX   Female
AG   35-39Y
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 19-12-24; Version: 12
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