Canonical Allele Identifier: PA2573275217
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472786
ClinVar RCV Id: RCV001969375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Pro297Ser
CA5543078
NM_018344.6:c.889C>T