Allele Registry

Canonical Allele Identifier: PA915971577

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012965

RCV000173141

RCV002307363

RCV002472929

ClinVar Variation:

12183

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.His63Leu	CA200316 NM_001128590.3:c.188A>T