Canonical Allele Identifier: PA2828087940
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1969970
ClinVar RCV Id: RCV002760283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.His190Tyr
CA377113860
NM_001363518.2:c.568C>T