Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100407357T>ACA316345PCDH19c.1241A>T (p.Glu414Val)
 ClinVar dbSNP
Xg.100407357T=CA2447976694PCDH19c.1241A= (p.Glu414=)
 dbSNP

Number of alleles fetched