Canonical Allele Identifier: PA2826692000
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 586612
ClinVar RCV Id: RCV000713346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Val132Met
CA397750116
NM_001284509.2:c.394G>A