Canonical Allele Identifier: PA2826692722
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 140754
ClinVar RCV Id: RCV000128862
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Leu445Pro
CA210616
NM_001284510.2:c.1334T>C