Allele Registry

Canonical Allele Identifier: PA2828286056

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000024069

RCV000029655

RCV000055819

RCV000252481

RCV001529036

ClinVar Variation:

12154

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Ser134Thr	CA129645 NM_001368144.1:c.401G>C