Canonical Allele Identifier: PA2828374968
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Arg266Trp
CA346983
NM_001370085.1:c.796C>T