Canonical Allele Identifier: PA2828087938
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 651684
ClinVar RCV Id: RCV000807094 RCV001090810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ala189Asp
CA5543059
NM_001363518.2:c.566C>A