Allele Registry

Canonical Allele Identifier: PA2826692666

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000202396

RCV003955216

ClinVar Variation:

218170

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271439.1:p.Ser384Leu	CA210672 NM_001284510.2:c.1151C>T