Canonical Allele Identifier: PA343797
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Leu339Pro
CA343794
NM_024531.5:c.1016T>C