Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.52452217C>ACA130608TNNC1c.91G>T (p.Ala31Ser)
c.-42G>T (n.-42G>T)
 ClinVar dbSNP
3g.52452217C>TCA297310TNNC1c.91G>A (p.Ala31Thr)
c.-42G>A (n.-42G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched