Canonical Allele Identifier: PA1139724047
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 969066
ClinVar RCV Id: RCV001244325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Asp292His
CA377114384
NM_018344.6:c.874G>C