Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
Y	g.640836C>T	CA212924		c.502C>T (p.Arg168Trp)	dbSNP
X	g.640836C>T	CA212923	SHOX	c.502C>T (p.Arg168Trp)	ClinVar dbSNP gnomAD v2 gnomAD v4
Y	g.640836C=	CA2467802549		c.502C= (p.Arg168=)	dbSNP

Number of alleles fetched