Canonical Allele Identifier: PA2828076525
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1723848
ClinVar RCV Id: RCV002306409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Ser52Pro
CA372626203
NM_001363120.2:c.154T>C