Canonical Allele Identifier: PA916065673
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 651684
ClinVar RCV Id: RCV000807094 RCV001090810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ala267Asp
CA5543059
NM_018344.6:c.800C>A