Canonical Allele Identifier: PA2828087956
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548284
ClinVar RCV Id: RCV003262976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ser215Thr
CA377114405
NM_001363518.2:c.643T>A