Canonical Allele Identifier: PA2828087935
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 300364
ClinVar RCV Id: RCV000365829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ala188Val
CA5543057
NM_001363518.2:c.563C>T