Canonical Allele Identifier: PA2826692007
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 660298
ClinVar RCV Id: RCV000817463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Leu139Phe
CA8331707
NM_001284509.2:c.417G>T
CA397750069
NM_001284509.2:c.417G>C