Allele Registry

Canonical Allele Identifier: PA2826483675

Gene: OASL HGNC NCBI

ClinVar RCV:

RCV004200472

ClinVar Variation:

2367928

HGVS (amino-acid)	Matching Registered Transcripts
NP_001248754.1:p.Ser279Thr	CA386950874 NM_001261825.2:c.836G>C