Canonical Allele Identifier: PA216166
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_001011554.1:p.Ile51Phe
CA216165
NM_001011554.3:c.151A>T