Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.134815629G>ACA322424COL5A1c.4068G>A (p.Ala1356=)
n.4470G>A
n.4466G>A
ClinVar dbSNP gnomAD v4
9g.134815629G=CA1883365595COL5A1c.4068G= (p.Ala1356=)
n.4470G=
n.4466G=
dbSNP

Number of alleles fetched