Canonical Allele Identifier: PA2828077413
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1466381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Gly177Ser
CA187657684
NM_001363122.2:c.529G>A