Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.45990792G>ACA257736COL6A1c.1022G>A (p.Gly341Asp)
 ClinVar dbSNP COSMIC
21g.45990792G>TCA10604208COL6A1c.1022G>T (p.Gly341Val)
 ClinVar dbSNP
21g.45990792G=CA2392434444COL6A1c.1022G= (p.Gly341=)
 dbSNP

Number of alleles fetched