Allele Registry

Canonical Allele Identifier: PA2829245987

Gene: OASL HGNC NCBI

ClinVar RCV:

RCV004080805

ClinVar Variation:

2216910

HGVS (amino-acid)	Matching Registered Transcripts
NP_001382348.1:p.Gly247Arg	CA6832813 NM_001395419.1:c.739G>C