Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38606743C>TCA014277SCN5Ac.1066G>A (p.Asp356Asn)
c.937G>A (p.Asp313Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38606743C>ACA352149609SCN5Ac.1066G>T (p.Asp356Tyr)
c.937G>T (p.Asp313Tyr)
 ClinVar dbSNP

Number of alleles fetched