Canonical Allele Identifier: PA2826692024
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 660383
ClinVar RCV Id: RCV000817564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Glu154Gly
CA397749976
NM_001284509.2:c.461A>G