Allele Registry

Canonical Allele Identifier: PA2826692267

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000128862

ClinVar Variation:

140754

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271438.1:p.Leu471Pro	CA210616 NM_001284509.2:c.1412T>C