Canonical Allele Identifier: PA2828375016
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002269
ClinVar RCV Id: RCV001298670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Gln322Arg
CA407962735
NM_001370085.1:c.965A>G