Canonical Allele Identifier: PA2828374874
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476610
ClinVar RCV Id: RCV000557473 RCV000825236 RCV001540821 RCV002377169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Arg132Gln
CA9724788
NM_001370085.1:c.395G>A