Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.52451799C>TCA297316TNNC1c.262G>A (p.Asp88Asn)
n.193G>A
c.130G>A (p.Asp44Asn)
 ClinVar dbSNP COSMIC
3g.52451799C>ACA353167291TNNC1c.262G>T (p.Asp88Tyr)
n.193G>T
c.130G>T (p.Asp44Tyr)
 ClinVar dbSNP

Number of alleles fetched