Canonical Allele Identifier: PA2826692716
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 475194
ClinVar RCV Id: RCV000525102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Ile440Val
CA8331368
NM_001284510.2:c.1318A>G