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QuickView for rs76754013;jsessionid=698F4D394307504BFD2EBF12B730DA2C (snp)


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      • Human Human A|C
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Type:
SNP
Organism:
Homo sapiens
Alleles:
A|C
Chromosomal Location:
chr 13 : 100626694 (build 36.3)
Strand:
+
Update Date:
Nov 14 2011
Associated Gene(s):
NALCN
Related URLs:
NCBI dbSNP


NALCN   (exon)  QuickView

Transcript CDS Change Protein Mutation Class AA Change
NM_052867
G1797T NP_443099 Missense L599F