Canonical Allele Identifier: PA2828375148
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1993579
ClinVar RCV Id: RCV002801504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Thr19Ile
CA407964629
NM_001370086.1:c.56C>T