Canonical Allele Identifier: PA2828375226
Gene: SLC52A3 HGNC NCBI
ClinVar RCV:
RCV000000164
ClinVar Variation:
141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Arg132Trp
CA339794
NM_001370086.1:c.394C>T