Search Results: 1 unique variant retrieved.
c.4979C>T
p.(Pro1660Leu) (Legacy AA No.1641)
Variant Type:
Point
Domain:
B
Sequence Context:
CCA > CTA
Variant Effect:
Missense
Location:
Exon 14
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
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