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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.5227019C>T
CA125383
HBB
c.3G>A (p.Met1Ile)
n.54G>A
ClinVar
dbSNP
11
g.5227019C>G
CA217115643
HBB
c.3G>C (p.Met1Ile)
n.54G>C
ClinVar
dbSNP
11
g.5227019C>A
CA217115639
HBB
c.3G>T (p.Met1Ile)
n.54G>T
ClinVar
dbSNP
Number of alleles fetched
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