Allele Registry

Canonical Allele Identifier: PA096205

Gene: SCO1 HGNC NCBI

ClinVar RCV:

RCV000006555

RCV001291618

ClinVar Variation:

6178

HGVS (amino-acid)	Matching Registered Transcripts
NP_004580.1:p.Pro174Leu	CA118051 NM_004589.4:c.521C>T