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Summary Attributions
XB-TRANSGENE-19776559

Transgene Name:

Tg(Hsa.SMCHD1G137E)
Description: Full length human SMCHD1 bearing a G137E substitution associated with BOSMA ARHINIA MICROPHTHALMIA SYNDROME (OMIM:603457)
Inducibility: None

Components
Name: smchd1_G137E
Type: ORF from genomic DNA
Sequence: No sequence available
Organism: Homo sapiens


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