Canonical Allele Identifier: PA2573307612
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515117
ClinVar RCV Id: RCV002020855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Arg37Ser
CA397752058
NM_177550.5:c.111G>T
CA397752061
NM_177550.5:c.111G>C