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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
3
g.129529002G>A
CA122823
RHO
c.269G>A (p.Gly90Asp)
ClinVar
dbSNP
3
g.129529002G>T
CA354496638
RHO
c.269G>T (p.Gly90Val)
dbSNP
gnomAD v4
3
g.129529002G=
CA1401205916
RHO
c.269G= (p.Gly90=)
dbSNP
Number of alleles fetched
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