Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
19	g.35848767C>T	CA250081	NPHS1	c.1040G>A (p.Gly347Glu) n.47G>A	ClinVar dbSNP
19	g.35848767C=	CA2333850557	NPHS1	c.1040G= (p.Gly347=) n.47G=	dbSNP

Number of alleles fetched