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QuickView for rs145707014;jsessionid=76EE01E4CCBF0B29556861ADB7061BF3 (snp)


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      • Human Human C|G
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Type:
SNP
Organism:
Homo sapiens
Alleles:
C|G
Chromosomal Location:
chr 12 : 73728279 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
KCNC2
Related URLs:
NCBI dbSNP


KCNC2   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_139136
C1701G NP_631874 Missense D567E
NM_139137
C1701G NP_631875 Missense D567E