Canonical Allele Identifier: PA2825857991
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501356
ClinVar RCV Id: RCV002042791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137310.1:p.Phe128Leu
CA397750247
NM_001143838.3:c.384C>G
CA397750248
NM_001143838.3:c.384C>A
CA397750253
NM_001143838.3:c.382T>C