Canonical Allele Identifier: PA891856412
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 572794
ClinVar RCV Id: RCV000694269
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Val407Met
CA5543153
NM_018344.6:c.1219G>A