Canonical Allele Identifier: PA2826179060
Gene: SLC13A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 64448
ClinVar RCV Id: RCV000054635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180269.1:p.Ile51Phe
CA216165
NM_001193340.2:c.151A>T