| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407902A>C | CA414008610 | PCDH19 | c.696T>G (p.Asn232Lys) | ClinVar dbSNP |
| X | g.100407902A>T | CA316321 | PCDH19 | c.696T>A (p.Asn232Lys) | ClinVar dbSNP |
| X | g.100407902A= | CA2447976916 | PCDH19 | c.696T= (p.Asn232=) | dbSNP |