Allele Registry

Canonical Allele Identifier: PA2826059670

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV000043620

RCV000872109

RCV001149870

RCV001149871

RCV002513637

ClinVar Variation:

50905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001162582.1:p.Arg114His	CA143840 NM_001169111.2:c.341G>A