Canonical Allele Identifier: PA2828375142
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 838277
ClinVar RCV Id: RCV001039792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Gly13Arg
CA9724838
NM_001370086.1:c.37G>A
CA310679445
NM_001370086.1:c.37G>C