Canonical Allele Identifier: PA1139748377
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 847825
ClinVar RCV Id: RCV001051448 RCV001552328 RCV002445268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Gly316Ser
CA9724643
NM_033409.4:c.946G>A