Canonical Allele Identifier: PA645502633
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 393192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Ala297Thr
CA16607815
NM_177550.5:c.889G>A