Canonical Allele Identifier: PA2741965649
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548287
ClinVar RCV Id: RCV003262979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ser293Tyr
CA377114420
NM_018344.6:c.878C>A