Canonical Allele Identifier: PA2580401170
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1902244
ClinVar RCV Id: RCV002580140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ala287Thr
CA377114262
NM_018344.6:c.859G>A