ID   GM21956
AC   CVCL_HK30
DR   Coriell; GM21956
DR   Wikidata; Q54852252
CC   Sequence variation: Mutation; HGNC; HGNC:3603; FBN1; Simple; p.Cys1672Phe (c.5015G>T); ClinVar=VCV000640108; Zygosity=Unspecified (Coriell=GM21956).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34807; Marfan syndrome
DI   ORDO; Orphanet_558; Marfan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   38Y
CA   Finite cell line
DT   Created: 01-12-16; Last updated: 19-12-24; Version: 11
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