Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154906468C>GCA255160F8c.5325G>C (p.Leu1775Phe)
c.5220G>C (p.Leu1740Phe)
ClinVar dbSNP
Xg.154906468C>TCA519357998F8c.5325G>A (p.Leu1775=)
c.5220G>A (p.Leu1740=)
dbSNP gnomAD v4
Xg.154906468C=CA2466828925F8c.5325G= (p.Leu1775=)
c.5220G= (p.Leu1740=)
dbSNP

Number of alleles fetched