Allele Registry

Canonical Allele Identifier: PA2825669238

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012961

RCV002472928

ClinVar Variation:

12179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Arg379Cys	CA3732711 NM_001128590.3:c.1135C>T