Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.46132125C>TCA208217COL6A2c.2633C>T (p.Ala878Val)
n.2710C>T
n.2717C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
21g.46132125C=CA2392512603COL6A2c.2633C= (p.Ala878=)
n.2710C=
n.2717C=
 dbSNP

Number of alleles fetched