Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100406916G>CCA316366PCDH19c.1682C>G (p.Pro561Arg)
 ClinVar dbSNP
Xg.100406916G>ACA414002193PCDH19c.1682C>T (p.Pro561Leu)
 ClinVar dbSNP

Number of alleles fetched