Canonical Allele Identifier: PA2828087949
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ser207Leu
CA5543065
NM_001363518.2:c.620C>T