Canonical Allele Identifier: PA916019720
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_001291391.1:p.Thr466Pro
CA364311409
NM_001304462.2:c.1396A>C