Canonical Allele Identifier: PA658828784
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 546412
ClinVar RCV Id: RCV000658283 RCV001301836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr162dup
CA8331704
NM_177550.5:c.485_487dup