Allele Registry

Canonical Allele Identifier: PA645465755

Gene: SCO1 HGNC NCBI

ClinVar RCV:

RCV000265637

RCV000324448

RCV002061215

RCV003137923

ClinVar Variation:

321791

HGVS (amino-acid)	Matching Registered Transcripts
NP_004580.1:p.Ile290Val	CA8393457 NM_004589.4:c.868A>G