Canonical Allele Identifier: PA2826692713
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372187
ClinVar RCV Id: RCV001872795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Ser437Pro
CA397738511
NM_001284510.2:c.1309T>C