Canonical Allele Identifier: PA916014259
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 218173
ClinVar RCV Id: RCV000202397 RCV003226911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Thr99Met
CA213347
NM_001284510.2:c.296C>T