Canonical Allele Identifier: PA916074807
Gene: SLC13A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 803301
ClinVar RCV Id: RCV000989689 RCV001557426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_808218.1:p.Thr145Met
CA397750140
NM_177550.5:c.434C>T