Canonical Allele Identifier: PA2826692754
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2095478
ClinVar RCV Id: RCV003013810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Phe498Ser
CA397737073
NM_001284510.2:c.1493T>C