Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.70175938G>CCA329705KCNJ2c.899G>C (p.Gly300Ala)
 ClinVar dbSNP gnomAD v4
17g.70175938G>ACA329702KCNJ2c.899G>A (p.Gly300Asp)
 ClinVar dbSNP
17g.70175938G>TCA254594KCNJ2c.899G>T (p.Gly300Val)
 ClinVar dbSNP

Number of alleles fetched