Canonical Allele Identifier: PA645375469
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 300364
ClinVar RCV Id: RCV000365829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060814.4:p.Ala266Val
CA5543057
NM_018344.6:c.797C>T