Canonical Allele Identifier: PA2826692116
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 393192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Ala280Thr
CA16607815
NM_001284509.2:c.838G>A