Canonical Allele Identifier: PA2499301603
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043572
ClinVar RCV Id: RCV001347701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr166Ala
CA397750006
NM_177550.5:c.496A>G