Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
19	g.35851260A>G	CA16041983	NPHS1	c.397+2T>C (n.397+2T>C)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19	g.35851260A>T	CA405410442	NPHS1	c.397+2T>A (n.397+2T>A)	ClinVar dbSNP

Number of alleles fetched