Canonical Allele Identifier: PA2828375390
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2610677
ClinVar RCV Id: RCV003378441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Val351Phe
CA407962556
NM_001370086.1:c.1051G>T