Allele Registry

Canonical Allele Identifier: PA103428

Gene: SLC29A3 HGNC NCBI

ClinVar RCV:

RCV000000599

RCV003398400

ClinVar Variation:

569

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