Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.20005878G>T	CA254203	MATN3	c.656C>A (p.Ala219Asp)	ClinVar dbSNP gnomAD v2 gnomAD v4
2	g.20005878G>A	CA345950642	MATN3	c.656C>T (p.Ala219Val)	dbSNP

Number of alleles fetched