Canonical Allele Identifier: PA2828088069
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2216320
ClinVar RCV Id: RCV002665727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Glu366Lys
CA377117361
NM_001363518.2:c.1096G>A