Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.68839731G>TCA121637EFNB1c.474G>T (p.Met158Ile)
ClinVar dbSNP
Xg.68839731G=CA2435564174EFNB1c.474G= (p.Met158=)
dbSNP
Xg.68839731G>ACA413438031EFNB1c.474G>A (p.Met158Ile)
ClinVar dbSNP

Number of alleles fetched