Correlation Engine 2.0
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QuickView for rs142606266;jsessionid=04DC2CA3A30C2E6D0D9AC64A44FC5488 (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 12 : 60388830 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
FAM19A2
Related URLs:
NCBI dbSNP


FAM19A2   (UTR)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_178539
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