Canonical Allele Identifier: PA2828375006
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210021
ClinVar RCV Id: RCV000191966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Ala312Val
CA346985
NM_001370085.1:c.935C>T