Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100407808C>GCA414008109PCDH19c.790G>C (p.Asp264His)
 ClinVar dbSNP
Xg.100407808C>ACA172968PCDH19c.790G>T (p.Asp264Tyr)
 ClinVar dbSNP

Number of alleles fetched