Canonical Allele Identifier: PA2828375378
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024926
ClinVar RCV Id: RCV001325168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Tyr334His
CA407962663
NM_001370086.1:c.1000T>C