ClinGen Allele Registry
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Canonical Allele Identifier:
PA103428
Gene: SLC29A3
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
15608
ClinVar RCV:
RCV000000599
RCV003398400
ClinVar Variation:
569
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_060814.4:p.Thr449Arg
CA114354
NM_018344.6:c.1346C>G