Canonical Allele Identifier: PA2828088090
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502661
ClinVar RCV Id: RCV002011045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ile397Thr
CA377118065
NM_001363518.2:c.1190T>C