Allele Registry

Canonical Allele Identifier: PA2826059565

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV002585822

ClinVar Variation:

1900684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162582.1:p.Arg20Leu	CA10321306 NM_001169111.2:c.59G>T