Data Export Options:
Search Results: 1 unique variant retrieved.
p.Gly138Asp (Legacy AA No. 78)
Variant Type:
Point
Domain:
EGF1
Sequence Context:
GGC > GAC
Variant Effect:
Missense
Location:
Exon (5)
No of bases:
1
No. of patients reported:
4
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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