Canonical Allele Identifier: PA2828087988
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906186
ClinVar RCV Id: RCV002588977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ile252Val
CA5543102
NM_001363518.2:c.754A>G