Allele Registry

Canonical Allele Identifier: PA2828286138

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012943

RCV000711371

RCV002288483

RCV003924827

RCV003985261

ClinVar Variation:

12159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Pro319Ser	CA341186 NM_001368144.1:c.955C>T