Canonical Allele Identifier: PA2829897978
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164067
ClinVar RCV Id: RCV004458955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ser419Asn
CA5543170
NM_018344.6:c.1256G>A