Canonical Allele Identifier: PA2826891977
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 429191
ClinVar RCV Id: RCV000492821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291395.1:p.Thr412Pro
CA364311409
NM_001304466.2:c.1234A>C