Allele Registry

Canonical Allele Identifier: PA2825669189

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000711388

RCV003317352

ClinVar Variation:

585757

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Leu278Val	CA136894756 NM_001128590.3:c.832T>G