Canonical Allele Identifier: PA2828088059
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037246
ClinVar RCV Id: RCV001340370 RCV004035936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Leu351Ile
CA5543175
NM_001363518.2:c.1051C>A