Data Display Options:

UNIQUE (Without Case Data) :
MULTIPLE (With Case Data) :

  Search Results: 1 unique variant retrieved.



  c.1858G>A
p.(Val620Met) (Legacy AA No.601)
Variant Type:
Point
Domain:
A2
Sequence Context:
GTG > ATG
Variant Effect:
Missense
Location:
Exon 12
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

Please click to see if there is the available information.

Individual Case Information : Show