Canonical Allele Identifier: PA2825455763
Gene: SLC29A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164053
ClinVar RCV Id: RCV004458941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001071643.1:p.Gly225Ser
CA3831636
NM_001078175.3:c.673G>A