Canonical Allele Identifier: PA2828087972
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047174
ClinVar RCV Id: RCV002904105 RCV004066204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Gly231Arg
CA5543088
NM_001363518.2:c.691G>C