Canonical Allele Identifier: PA2825858124
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 393192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Ala297Thr
CA16607815
NM_001143838.3:c.889G>A