Canonical Allele Identifier: PA103428
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 569
ClinVar RCV Id: RCV000000599 RCV003398400
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Thr449Arg
CA114354
NM_018344.6:c.1346C>G