Canonical Allele Identifier: PA2828087960
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1382317
ClinVar RCV Id: RCV001897582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Arg221His
CA5543082
NM_001363518.2:c.662G>A