Canonical Allele Identifier: PA2828077414
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Leu178Pro
CA372628864
NM_001363122.2:c.533T>C