Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.110192257C>ACA341454COL4A1c.1493G>T (p.Gly498Val)
n.1623G>T
c.1301G>T (p.Gly434Val)
ClinVar dbSNP
13g.110192257C>TCA388723400COL4A1c.1493G>A (p.Gly498Asp)
n.1623G>A
c.1301G>A (p.Gly434Asp)
ClinVar dbSNP

Number of alleles fetched