Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.100408229G>T	CA316287	PCDH19	c.369C>A (p.Asn123Lys)	ClinVar dbSNP
X	g.100408229G>A	CA333826100	PCDH19	c.369C>T (p.Asn123=)	ClinVar dbSNP gnomAD v4 COSMIC
X	g.100408229G>C	CA414010286	PCDH19	c.369C>G (p.Asn123Lys)	ClinVar dbSNP

Number of alleles fetched