Canonical Allele Identifier: PA2828087964
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379589
ClinVar RCV Id: RCV001914889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Ile223Asn
CA377114578
NM_001363518.2:c.668T>A