Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.38352774G>TCA224774OTCc.77+1G>T (p.=)
c.172-313347G>T (p.=)
n.169+1G>T
ClinVar dbSNP
Xg.38352774G>ACA224773OTCc.77+1G>A (p.=)
c.172-313347G>A (p.=)
n.169+1G>A
ClinVar dbSNP

Number of alleles fetched