Canonical Allele Identifier: PA103428
Gene: SLC29A3 HGNC NCBI
ClinVar Allele:
ClinVar Variation:

Amino-acid Alleles

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