Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
19	g.35284953C>G	CA405301171	HAMP	c.166C>G (p.Arg56Gly) n.2437C>G	dbSNP
19	g.35284953C>T	CA253053	HAMP	c.166C>T (p.Arg56Ter) n.2437C>T	ClinVar dbSNP gnomAD v4 COSMIC

Number of alleles fetched