Allele Registry

Canonical Allele Identifier: PA2826059652

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV001971786

ClinVar Variation:

1477832

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