Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.69616491C>T	CA517051650	EDA	c.183C>T (p.Tyr61=) n.425C>T n.406C>T	ClinVar dbSNP gnomAD v4
X	g.69616491C>G	CA255658	EDA	c.183C>G (p.Tyr61Ter) n.425C>G n.406C>G	ClinVar dbSNP

Number of alleles fetched