Allele Registry

Canonical Allele Identifier: PA321055

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV001971786

ClinVar Variation:

1477832

HGVS (amino-acid)	Matching Registered Transcripts
NP_005129.2:p.Arg95Cys	CA321053 NM_005138.3:c.283C>T