Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.5558G>T
p.Gly1853Val (Legacy AA No. 1825)
Variant Type: 
Point
Domain: 
d5A3
Location: 
Exon 17
Variant Effect: 
Missense
Codon Change: 
5558G>T
No. of Patients Reported: 
3
Phenotype: 
NA
Association: 
Unknown
Allele Count *: 
361
Allele Number *: 
282286
Allele Frequency *: 
0.001279
References and Comments:
NCBI Clinvar Variation ID: 293580NA