Canonical Allele Identifier: PA891856400
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 566799
ClinVar RCV Id: RCV000686712 RCV002544758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ser288Thr
CA5543069
NM_018344.6:c.862T>A