Canonical Allele Identifier: PA645502629
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 426419
ClinVar RCV Id: RCV000489414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Ala178_Lys179dup
CA645293897
NM_177550.5:c.533_538dup