List of variants in gene SLC24A1 reported as pathogenic for inborn disorder of amino acid metabolism

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004727.3(SLC24A1):c.754_755del (p.Met252fs)	rs777989874	0.00016
NM_004727.3(SLC24A1):c.95T>A (p.Leu32Ter)	rs1566945534

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