Canonical Allele Identifier: PA1139757133
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 846566
ClinVar RCV Id: RCV001049896 RCV001574963 RCV003307852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Gly169Ser
CA8331696
NM_177550.5:c.505G>A