Canonical Allele Identifier: PA2499284834
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023478
ClinVar RCV Id: RCV001323522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ala267Thr
CA377113844
NM_018344.6:c.799G>A