Allele Registry

Canonical Allele Identifier: PA2825669163

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000169566

RCV000711384

ClinVar Variation:

189145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.[Ile207_Val208delinsAsnGlu;Met210Lys]	CA274415 NM_001128590.3:c.620_629delinsACGAGGAGAA CA358448 NM_001128590.3:c.[620T>A;623T>A;629T>A]