Canonical Allele Identifier: PA2573194958
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_001271439.1:p.Phe85Leu
CA397750247
NM_001284510.2:c.255C>G
CA397750248
NM_001284510.2:c.255C>A
CA397750253
NM_001284510.2:c.253T>C