Canonical Allele Identifier: PA2828088073
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 569
ClinVar RCV Id: RCV000000599 RCV003398400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Thr371Arg
CA114354
NM_001363518.2:c.1112C>G