Canonical Allele Identifier: PA2826692535
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043572
ClinVar RCV Id: RCV001347701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Thr123Ala
CA397750006
NM_001284510.2:c.367A>G