Canonical Allele Identifier: PA2828375252
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744875
ClinVar RCV Id: RCV002335604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Asn168His
CA407963708
NM_001370086.1:c.502A>C