Canonical Allele Identifier: PA2580536549
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2091089
ClinVar RCV Id: RCV002991531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Met525Leu
CA397737909
NM_177550.5:c.1573A>T
CA397737914
NM_177550.5:c.1573A>C