Allele Registry

Canonical Allele Identifier: PA2580295232

Gene: OASL HGNC NCBI

ClinVar RCV:

RCV004200472

ClinVar Variation:

2367928

HGVS (amino-acid)	Matching Registered Transcripts
NP_003724.1:p.Ser409Thr	CA386950874 NM_003733.4:c.1226G>C