Canonical Allele Identifier: PA2826692538
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Val130Met
CA397749966
NM_001284510.2:c.388G>A