Canonical Allele Identifier: PA2828076575
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014285
ClinVar RCV Id: RCV001312997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.His110Tyr
CA372626850
NM_001363120.2:c.328C>T