Canonical Allele Identifier: PA2826692397
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 393192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Ala254Thr
CA16607815
NM_001284510.2:c.760G>A