Canonical Allele Identifier: PA2828375282
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Arg212Cys
CA347001
NM_001370086.1:c.634C>T