Canonical Allele Identifier: PA1139757025
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 966392
ClinVar RCV Id: RCV001241055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr166Asn
CA8331699
NM_177550.5:c.497C>A