Allele Registry

Canonical Allele Identifier: PA2826059267

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV002617549

ClinVar Variation:

1922517

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162581.1:p.Arg20Gln	CA10321307 NM_001169110.1:c.59G>A