Canonical Allele Identifier: PA2826692348
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 660383
ClinVar RCV Id: RCV000817564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Glu128Gly
CA397749976
NM_001284510.2:c.383A>G