Canonical Allele Identifier: PA2826108631
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 287285
ClinVar RCV Id: RCV000389149 RCV000644615 RCV001701933 RCV002519284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167569.1:p.Leu43Arg
CA5542824
NM_001174098.2:c.128T>G