Canonical Allele Identifier: PA2828375372
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305596
ClinVar RCV Id: RCV001768803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Ser328Phe
CA407962694
NM_001370086.1:c.983C>T