Canonical Allele Identifier: PA916074872
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 659306
ClinVar RCV Id: RCV000816292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Arg481Cys
CA8331370
NM_177550.5:c.1441C>T