Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154997065A>TCA255054F8c.296T>A (p.Val99Asp)
c.*82T>A (n.*82T>A)
c.191T>A (p.Val64Asp)
c.278T>A (p.Val93Asp)
ClinVar dbSNP
Xg.154997065A>GCA414920067F8c.296T>C (p.Val99Ala)
c.*82T>C (n.*82T>C)
c.191T>C (p.Val64Ala)
c.278T>C (p.Val93Ala)
ClinVar dbSNP

Number of alleles fetched