Allele Registry

Canonical Allele Identifier: PA2825669199

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV003318405

ClinVar Variation:

1341485

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Arg310His	CA3732614 NM_001128590.3:c.929G>A