Canonical Allele Identifier: PA2826692146
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2140104
ClinVar RCV Id: RCV003052947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Pro322Thr
CA397743738
NM_001284509.2:c.964C>A