Product Details

SNP ID
rs13477725
Assay Type
Pre Designed
NCBI dbSNP Submissions
NA
Location
Chr.4:57613710 on Build GRCm38
Set Membership
Context Sequence [VIC/FAM]
AAAATGAATTTAGAGTGCAGCTCTG[C/T]TTGTGGTTTTTCAGCCGTAAGTATT
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
Palm2 PubMed Links

Gene Details

Gene
Palm2
Gene Name
paralemmin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_172868.3 Intron NP_766456.1

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