Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100408135C>GCA414009592PCDH19c.463G>C (p.Asp155His)
 ClinVar dbSNP
Xg.100408135C>TCA316298PCDH19c.463G>A (p.Asp155Asn)
 ClinVar dbSNP COSMIC

Number of alleles fetched