Canonical Allele Identifier: PA2573275214
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427091
ClinVar RCV Id: RCV001949893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Pro297Leu
CA377114502
NM_018344.6:c.890C>T