Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561902C>TCA255405F9c.1217C>T (p.Ser406Leu)
n.1723+161C>T
c.1103C>T (p.Ser368Leu)
c.1088C>T (p.Ser363Leu)
ClinVar dbSNP
Xg.139561902C=CA2461412230F9c.1217C= (p.Ser406=)
n.1723+161C=
c.1103C= (p.Ser368=)
c.1088C= (p.Ser363=)
dbSNP

Number of alleles fetched