Canonical Allele Identifier: PA2825858074
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675654
ClinVar RCV Id: RCV002211383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Gly226Arg
CA8331651
NM_001143838.3:c.676G>A
CA397748820
NM_001143838.3:c.676G>C