Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.886G>A
p.Ala296Thr (Legacy AA No. 268)
Variant Type: 
Point
Domain: 
d5A1
Location: 
Exon 6
Variant Effect: 
Missense
Codon Change: 
886G>A
No. of Patients Reported: 
2
Phenotype: 
NA
Association: 
Unknown
Allele Count *: 
6
Allele Number *: 
282804
Allele Frequency *: 
0.000021
References and Comments:
NCBI Clinvar Variation ID: 293634NA