Allele Registry

Canonical Allele Identifier: PA2825669272

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000243232

ClinVar Variation:

193596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Ser464Asn	CA239138 NM_001128590.3:c.1391G>A