Canonical Allele Identifier: PA916049777
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 648925
ClinVar RCV Id: RCV000803756 RCV001797145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Arg268Gln
CA9724676
NM_033409.4:c.803G>A