Canonical Allele Identifier: PA2826692746
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2091089
ClinVar RCV Id: RCV002991531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Met482Leu
CA397737909
NM_001284510.2:c.1444A>T
CA397737914
NM_001284510.2:c.1444A>C