Canonical Allele Identifier: PA658819753
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 521339
ClinVar RCV Id: RCV000622896 RCV001868146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Cys386Arg
CA407962325
NM_033409.4:c.1156T>C