Canonical Allele Identifier: PA346984
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210020
ClinVar RCV Id: RCV000191965 RCV000483942 RCV002415816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Arg266Trp
CA346983
NM_033409.4:c.796C>T