Canonical Allele Identifier: PA1139752651
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 860801
ClinVar RCV Id: RCV001067177 RCV002374979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Gln298Arg
CA4938305
NM_024531.5:c.893A>G