Canonical Allele Identifier: PA645375487
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 300367
ClinVar RCV Id: RCV000332292 RCV003417973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Phe316Val
CA5543092
NM_018344.6:c.946T>G