Canonical Allele Identifier: PA2499301601
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1048670
ClinVar RCV Id: RCV001712895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr145Lys
CA397750142
NM_177550.5:c.434C>A