Allele Registry

Canonical Allele Identifier: PA2828286073

Gene: CYP21A2 HGNC NCBI

ClinVar Allele:

976290

ClinVar RCV:

RCV001269684

ClinVar Variation:

988370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Gln184Glu	CA363510515 NM_001368144.1:c.550C>G