Canonical Allele Identifier: PA103428
Gene: SLC29A3 HGNC NCBI
ClinVar Allele:
15608
ClinVar RCV:
RCV000000599
RCV003398400
ClinVar Variation:
569
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Amino-acid Alleles

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