Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.219418500C>T	CA261520	DES	c.38C>T (p.Ser13Phe)	ClinVar dbSNP
2	g.219418500C>A	CA350682283	DES	c.38C>A (p.Ser13Tyr)	ClinVar dbSNP

Number of alleles fetched