Allele Registry

Canonical Allele Identifier: PA2829245966

Gene: OASL HGNC NCBI

ClinVar RCV:

RCV004167463

ClinVar Variation:

2325339

HGVS (amino-acid)	Matching Registered Transcripts
NP_001382347.1:p.Ala180Ser	CA386959084 NM_001395418.1:c.538G>T