Canonical Allele Identifier: PA2826692260
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 475195
ClinVar RCV Id: RCV000555123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271438.1:p.Gly467Ser
CA8331365
NM_001284509.2:c.1399G>A