Canonical Allele Identifier: PA2828087958
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427091
ClinVar RCV Id: RCV001949893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Pro219Leu
CA377114502
NM_001363518.2:c.656C>T