Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1300G>A
p.Val434Met (Legacy AA No. 406)
Variant Type: 
Point
Domain: 
d5A2
Location: 
Exon 9
Variant Effect: 
Missense
Codon Change: 
1300G>A
No. of Patients Reported: 
2
Phenotype: 
NA
Association: 
Unknown
Allele Count *: 
15
Allele Number *: 
282614
Allele Frequency *: 
0.000053
References and Comments:
NCBI Clinvar Variation ID: 293630NA