Canonical Allele Identifier: PA2826691995
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1048670
ClinVar RCV Id: RCV001712895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Thr128Lys
CA397750142
NM_001284509.2:c.383C>A