Allele Registry

Canonical Allele Identifier: PA915989132

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV000006034

RCV001851687

ClinVar Variation:

5680

HGVS (amino-acid)	Matching Registered Transcripts
NP_005129.2:p.Arg171Trp	CA117676 NM_005138.3:c.511C>T