Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38587545A>GCA016037SCN5Ac.2291T>C (p.Met764Thr)
c.2162T>C (p.Met721Thr)
 ClinVar dbSNP gnomAD v4
3g.38587545A>CCA016048SCN5Ac.2291T>G (p.Met764Arg)
c.2162T>G (p.Met721Arg)
 ClinVar dbSNP

Number of alleles fetched