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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.110192257C>A
CA341454
COL4A1
c.1493G>T (p.Gly498Val)
n.1623G>T
c.1301G>T (p.Gly434Val)
ClinVar
dbSNP
13
g.110192257C>T
CA388723400
COL4A1
c.1493G>A (p.Gly498Asp)
n.1623G>A
c.1301G>A (p.Gly434Asp)
ClinVar
dbSNP
Number of alleles fetched
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