Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154906470A>CCA255159F8c.5323T>G (p.Leu1775Val)
c.5218T>G (p.Leu1740Val)
 ClinVar dbSNP
Xg.154906470A=CA2466828926F8c.5323T= (p.Leu1775=)
c.5218T= (p.Leu1740=)
 dbSNP

Number of alleles fetched