Allele Registry

Canonical Allele Identifier: PA210617

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000128862

ClinVar Variation:

140754

HGVS (amino-acid)	Matching Registered Transcripts
NP_808218.1:p.Leu488Pro	CA210616 NM_177550.5:c.1463T>C