Canonical Allele Identifier: PA2828374892
Gene: SLC52A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357014.1:p.Gly160Ser
CA9724771
NM_001370085.1:c.478G>A