Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.173903978C>TCA210746SERPINC1c.1306G>A (p.Ala436Thr)
c.691G>A (p.Ala231Thr)
c.1162G>A (p.Ala388Thr)
c.1429G>A (p.Ala477Thr)
c.1387G>A (p.Ala463Thr)
c.1285G>A (p.Ala429Thr)
c.1249G>A (p.Ala417Thr)
c.1090G>A (p.Ala364Thr)
ClinVar dbSNP
1g.173903978C=CA1141581228SERPINC1c.1306G= (p.Ala436=)
c.691G= (p.Ala231=)
c.1162G= (p.Ala388=)
c.1429G= (p.Ala477=)
c.1387G= (p.Ala463=)
c.1285G= (p.Ala429=)
c.1249G= (p.Ala417=)
c.1090G= (p.Ala364=)
dbSNP

Number of alleles fetched