Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.63957473G>TCA341669SCN4Ac.2065C>A (p.Leu689Ile)
 ClinVar dbSNP gnomAD v4
17g.63957473G>ACA400631288SCN4Ac.2065C>T (p.Leu689Phe)
 ClinVar dbSNP

Number of alleles fetched