Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51790450C>TCA318284SCN8Ac.4472C>T (p.Ala1491Val)
c.2536C>T
c.4349C>T (p.Ala1450Val)
c.4505C>T (p.Ala1502Val)
ClinVar dbSNP COSMIC COSMIC
12g.51790450C=CA2036173498SCN8Ac.4472C= (p.Ala1491=)
c.2536C=
c.4349C= (p.Ala1450=)
c.4505C= (p.Ala1502=)
dbSNP

Number of alleles fetched