Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
15	g.73329719C>T	CA202778	HCN4	c.1444G>A (p.Gly482Arg) c.226G>A (p.Gly76Arg)	ClinVar dbSNP
15	g.73329719C>G	CA16043942	HCN4	c.1444G>C (p.Gly482Arg) c.226G>C (p.Gly76Arg)	ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched