Allele Registry

Canonical Allele Identifier: PA2826692210

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000202396

RCV003955216

ClinVar Variation:

218170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271438.1:p.Ser410Leu	CA210672 NM_001284509.2:c.1229C>T