| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407891G>C | CA16616407 | PCDH19 | c.707C>G (p.Pro236Arg) | ClinVar dbSNP |
| X | g.100407891G>A | CA414008536 | PCDH19 | c.707C>T (p.Pro236Leu) | ClinVar dbSNP COSMIC |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.100407891G>C | CA16616407 | PCDH19 | c.707C>G (p.Pro236Arg) | ClinVar dbSNP |
| X | g.100407891G>A | CA414008536 | PCDH19 | c.707C>T (p.Pro236Leu) | ClinVar dbSNP COSMIC |