Allele Registry

Canonical Allele Identifier: PA322392

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV000197926

RCV001149868

RCV001149869

RCV002517259

ClinVar Variation:

215130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162580.1:p.Arg179Cys	CA322391 NM_001169109.2:c.535C>T