Canonical Allele Identifier: PA2826692453
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 946341
ClinVar RCV Id: RCV001217187 RCV003442776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Arg506Gln
CA8331301
NM_001284510.2:c.1517G>A