Allele Registry

Canonical Allele Identifier: PA108878

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV000006038

ClinVar Variation:

5684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162580.1:p.Cys133Tyr	CA117681 NM_001169109.2:c.398G>A