Canonical Allele Identifier: PA2828076732
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393472
ClinVar RCV Id: RCV001908603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350049.1:p.Cys278Phe
CA372628064
NM_001363120.2:c.833G>T