Allele Registry

Canonical Allele Identifier: PA341187

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012943

RCV000711371

RCV002288483

RCV003924827

RCV003985261

ClinVar Variation:

12159

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Pro454Ser	CA341186 NM_000500.9:c.1360C>T