Canonical Allele Identifier: PA916043748
Gene: SLC29A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 568
ClinVar RCV Id: RCV000000598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350447.1:p.Met38Arg
CA114353
NM_001363518.2:c.113T>G