Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.68839731G>T | CA121637 | EFNB1 | c.474G>T (p.Met158Ile) | ClinVar dbSNP |
X | g.68839731G= | CA2435564174 | EFNB1 | c.474G= (p.Met158=) | dbSNP |
X | g.68839731G>A | CA413438031 | EFNB1 | c.474G>A (p.Met158Ile) | ClinVar dbSNP |