Allele Registry

Canonical Allele Identifier: PA2828286087

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012937

RCV000711368

RCV003407321

ClinVar Variation:

12152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Arg222Trp	CA341181 NM_001368144.1:c.664C>T