Canonical Allele Identifier: PA2826692108
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 651382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Gly271Arg
CA8331580
NM_001284509.2:c.811G>A
CA287388259
NM_001284509.2:c.811G>C