Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100407903T>CCA316319PCDH19c.695A>G (p.Asn232Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.100407903T>ACA172965PCDH19c.695A>T (p.Asn232Ile)
 ClinVar dbSNP
Xg.100407903T=CA2447976917PCDH19c.695A= (p.Asn232=)
 dbSNP

Number of alleles fetched