Product Details
- SNP ID
-
rs5977126
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:129648559 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCAGTGATGAGCGGCAGGATCACCC[A/G]GCTTCTAGGCTGTCCTTCTCCCTCC
- Phenotype
-
MIM: 300297
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
APLN
PubMed Links
Gene Details
- Gene
- APLN
- Gene Name
- apelin
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_017413.4 |
|
Intron |
|
|
NP_059109.3 |
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