Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.5723G>A
p.Arg1908Lys (Legacy AA No. 1880)
Variant Type: 
Point
Domain: 
d5C1
Location: 
Exon 19
Variant Effect: 
Missense
Codon Change: 
5723G>A
No. of Patients Reported: 
1
Phenotype: 
NA
Association: 
Unknown
Allele Count *: 
264
Allele Number *: 
282114
Allele Frequency *: 
0.000936
References and Comments:
NCBI Clinvar Variation ID: 709012NA