Canonical Allele Identifier: PA2828375367
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357015.1:p.Pro319Ser
CA346987
NM_001370086.1:c.955C>T