Canonical Allele Identifier: PA658673180
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 475195
ClinVar RCV Id: RCV000555123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Gly484Ser
CA8331365
NM_177550.5:c.1450G>A