Canonical Allele Identifier: PA346968
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210011
ClinVar RCV Id: RCV000191956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_212134.3:p.Trp17Arg
CA346967
NM_033409.4:c.49T>C
CA407964647
NM_033409.4:c.49T>A