Canonical Allele Identifier: PA2826891960
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429191
ClinVar RCV Id: RCV000492821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291394.1:p.Thr413Pro
CA364311409
NM_001304465.2:c.1237A>C