Allele Registry

Canonical Allele Identifier: PA2825669194

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001269684

ClinVar Variation:

988370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gln289Glu	CA363510515 NM_001128590.3:c.865C>G