Allele Registry

Canonical Allele Identifier: PA2580326964

Gene: SCO2 HGNC NCBI

ClinVar RCV:

RCV002585822

ClinVar Variation:

1900684

HGVS (amino-acid)	Matching Registered Transcripts
NP_005129.2:p.Arg20Leu	CA10321306 NM_005138.3:c.59G>T