Canonical Allele Identifier: PA210668
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 140753
ClinVar RCV Id: RCV000128861 RCV000826127 RCV001701766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr227Met
CA210667
NM_177550.5:c.680C>T