Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
1	g.179564715G>A	CA351864	NPHS2	c.353C>T (p.Pro118Leu) c.275-4954C>T (n.275-4954C>T)	ClinVar dbSNP gnomAD v4 COSMIC
1	g.179564715G=	CA1210322092	NPHS2	c.353C= (p.Pro118=) c.275-4954C= (n.275-4954C=)	dbSNP

Number of alleles fetched