Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154896228T>CCA255201F8c.6278A>G (p.Asp2093Gly)
c.6173A>G (p.Asp2058Gly)
 ClinVar dbSNP
Xg.154896228T>ACA414900400F8c.6278A>T (p.Asp2093Val)
c.6173A>T (p.Asp2058Val)
 ClinVar dbSNP

Number of alleles fetched