Allele Registry

Canonical Allele Identifier: PA2825669210

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012937

RCV000711368

RCV003407321

ClinVar Variation:

12152

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Arg327Trp	CA341181 NM_001128590.3:c.979C>T