Canonical Allele Identifier: PA2828375377
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2052671
ClinVar RCV Id: RCV002937622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Val332Ala
CA9724634
NM_001370086.1:c.995T>C