Canonical Allele Identifier: PA2826059597
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 900447
ClinVar RCV Id: RCV001145653 RCV001145652 RCV001858956 RCV002559406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Arg58Gln
CA10321280
NM_001169111.2:c.173G>A