Canonical Allele Identifier: PA2828077410
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350051.1:p.Leu175Pro
CA343794
NM_001363122.2:c.524T>C