Canonical Allele Identifier: PA2826059652
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477832
ClinVar RCV Id: RCV001971786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Arg95Cys
CA321053
NM_001169111.2:c.283C>T