Canonical Allele Identifier: PA2828076560
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 840383
ClinVar RCV Id: RCV001042355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Thr92Ile
CA372626670
NM_001363120.2:c.275C>T