ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826130927
Gene: SLC34A2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
5717
ClinVar RCV Id:
RCV000006071
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001171469.2:p.Gly105Arg
CA117705
NM_001177998.2:c.313G>C
CA2879413
NM_001177998.2:c.313G>A