Search Results: 1 unique variant retrieved.
c.701C>G
p.(Ser234Cys) (Legacy AA No.215)
Variant Type:
Point
Domain:
A1
Sequence Context:
TCC > TGC
Variant Effect:
Missense
Location:
Exon 6
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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