Canonical Allele Identifier: PA2828375229
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210031
ClinVar RCV Id: RCV000191976 RCV001753593 RCV002354539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Thr135Ala
CA346999
NM_001370086.1:c.403A>G