Canonical Allele Identifier: PA2825858000
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 218173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Thr142Met
CA213347
NM_001143838.3:c.425C>T