Canonical Allele Identifier: PA645376219
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 262240
ClinVar RCV Id: RCV000250284 RCV001523331 RCV001640575 RCV002500928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Thr278Met
CA9724670
NM_033409.4:c.833C>T