Allele Registry

Canonical Allele Identifier: PA2826692726

Gene: SLC13A5 HGNC NCBI

ClinVar RCV:

RCV000416419

ClinVar Variation:

375390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271439.1:p.Leu449Pro	CA16044235 NM_001284510.2:c.1346T>C