Canonical Allele Identifier: PA2573275220
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1382317
ClinVar RCV Id: RCV001897582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Arg299His
CA5543082
NM_018344.6:c.896G>A