Canonical Allele Identifier: PA2573095755
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313440
ClinVar RCV Id: RCV001763804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078807.1:p.Ala124Thr
CA372626979
NM_024531.5:c.370G>A