Canonical Allele Identifier: PA2828087953
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 859278
ClinVar RCV Id: RCV001065349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ile213Thr
CA5543073
NM_001363518.2:c.638T>C