Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.100406927G>CCA121303PCDH19c.1671C>G (p.Asn557Lys)
 ClinVar dbSNP
Xg.100406927G>ACA517747623PCDH19c.1671C>T (p.Asn557=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC

Number of alleles fetched