Canonical Allele Identifier: PA2828088047
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1054535
ClinVar RCV Id: RCV001363056 RCV001729856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Asp334Gly
CA5543160
NM_001363518.2:c.1001A>G