Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.149483006G>ACA349672IDSc.1393C>T (p.Gln465Ter)
c.760C>T (p.Gln254Ter)
c.1123C>T (p.Gln375Ter)
 ClinVar dbSNP
Xg.149483006G>TCA16608716IDSc.1393C>A (p.Gln465Lys)
c.760C>A (p.Gln254Lys)
c.1123C>A (p.Gln375Lys)
 ClinVar dbSNP

Number of alleles fetched