Allele Registry

Canonical Allele Identifier: PA2828286066

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211046

RCV002281650

ClinVar Variation:

1675317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Val170Met	CA3732569 NM_001368144.1:c.508G>A