Canonical Allele Identifier: PA2828375317
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761029
ClinVar RCV Id: RCV002416572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.His263Arg
CA407963095
NM_001370086.1:c.788A>G