Canonical Allele Identifier: PA2826692525
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1992657
ClinVar RCV Id: RCV002796084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271439.1:p.Val109Leu
CA397750097
NM_001284510.2:c.325G>T
CA397750098
NM_001284510.2:c.325G>C