Allele Registry

Canonical Allele Identifier: PA2826483670

Gene: OASL HGNC NCBI

ClinVar RCV:

RCV004167463

ClinVar Variation:

2325339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001248754.1:p.Ala180Ser	CA386959084 NM_001261825.2:c.538G>T