Allele Registry

Canonical Allele Identifier: PA2825669188

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211047

RCV002473356

ClinVar Variation:

1675318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Phe277Val	CA3732571 NM_001128590.3:c.829T>G