List of variants reported as likely pathogenic for neuronal ceroid lipofuscinosis by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001042432.2(CLN3):c.512C>T (p.Ser171Phe)	rs1401497994
NM_001371596.2(MFSD8):c.416G>T (p.Arg139Leu)
NM_153033.5(KCTD7):c.793G>A (p.Gly265Arg)	rs200415747

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