Allele Registry

Canonical Allele Identifier: PA2828285931

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000169566

RCV000711384

ClinVar Variation:

189145

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355072.1:p.[Ile102_Val103delinsAsnGlu;Met105Lys]	CA274415 NM_001368143.1:c.305_314delinsACGAGGAGAA CA358448 NM_001368143.1:c.[305T>A;308T>A;314T>A]