Canonical Allele Identifier: PA2828076533
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1493748
ClinVar RCV Id: RCV001986713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Asn59Ser
CA372626289
NM_001363120.2:c.176A>G