Canonical Allele Identifier: PA2828076969
Gene: SLC52A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797154
ClinVar RCV Id: RCV002437779 RCV003102820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350050.1:p.Ala96Val
CA372626701
NM_001363121.2:c.287C>T