Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.139561916A>GCA255441F9c.1231A>G (p.Ser411Gly)
n.1723+175A>G
c.1117A>G (p.Ser373Gly)
c.1102A>G (p.Ser368Gly)
ClinVar dbSNP
Xg.139561916A=CA2461412241F9c.1231A= (p.Ser411=)
n.1723+175A=
c.1117A= (p.Ser373=)
c.1102A= (p.Ser368=)
dbSNP

Number of alleles fetched