Allele Registry

Canonical Allele Identifier: PA108866

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV000006034

RCV001851687

ClinVar Variation:

5680

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162580.1:p.Arg171Trp	CA117676 NM_001169109.2:c.511C>T