Canonical Allele Identifier: PA2828076586
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39576
ClinVar RCV Id: RCV000032776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Leu123Pro
CA343790
NM_001363120.2:c.368T>C