Canonical Allele Identifier: PA2742021569
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2546282
ClinVar RCV Id: RCV003292650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Val522Phe
CA397737954
NM_177550.5:c.1564G>T