Canonical Allele Identifier: PA2828087957
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472786
ClinVar RCV Id: RCV001969375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Pro219Ser
CA5543078
NM_001363518.2:c.655C>T