Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.50592063G>A | CA10603595 | CACNA1G | c.2881G>A (p.Ala961Thr) n.3273G>A c.2830G>A (p.Ala944Thr) n.3626G>A | ClinVar dbSNP |
17 | g.50592063G= | CA2264100278 | CACNA1G | c.2881G= (p.Ala961=) n.3273G= c.2830G= (p.Ala944=) n.3626G= | dbSNP |