Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.68839753C>TCA150571EFNB1c.496C>T (p.Gln166Ter)
 ClinVar dbSNP
Xg.68839753C=CA2435564179EFNB1c.496C= (p.Gln166=)
 dbSNP

Number of alleles fetched