Canonical Allele Identifier: PA2828076587
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313440
ClinVar RCV Id: RCV001763804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ala124Thr
CA372626979
NM_001363120.2:c.370G>A