Allele Registry

Canonical Allele Identifier: PA117678

Gene: SCO2 HGNC NCBI

ClinVar Allele:

20720

ClinVar RCV:

RCV000006035

RCV000043619

RCV000198477

RCV000626777

RCV001610286

ClinVar Variation:

5681

HGVS (amino-acid)	Matching Registered Transcripts
NP_005129.2:p.Glu140Lys	CA117677 NM_005138.3:c.418G>A