Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.69616472T>ACA261482EDAc.164T>A (p.Leu55Gln)
n.406T>A
n.387T>A
 ClinVar dbSNP
Xg.69616472T=CA2435839533EDAc.164T= (p.Leu55=)
n.406T=
n.387T=
 dbSNP

Number of alleles fetched