Search Results: 1 unique variant retrieved.
c.86T>G
p.(Val29Gly) (Legacy AA No.10)
Variant Type:
Point
Domain:
A1
Sequence Context:
GTG > GGG
Variant Effect:
Missense
Location:
Exon 1
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show