Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.68839664C>TCA16043923EFNB1c.407C>T (p.Ser136Leu)
ClinVar dbSNP
Xg.68839664C=CA2435564150EFNB1c.407C= (p.Ser136=)
dbSNP

Number of alleles fetched