Allele Registry

Canonical Allele Identifier: PA2826692722

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000128862

ClinVar Variation:

140754

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271439.1:p.Leu445Pro	CA210616 NM_001284510.2:c.1334T>C