ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826692348
Gene: SLC13A5
HGNC
NCBI
Linked Data
ClinVar Variation Id:
660383
ClinVar RCV Id:
RCV000817564
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001271439.1:p.Glu128Gly
CA397749976
NM_001284510.2:c.383A>G