Allele Registry

Canonical Allele Identifier: PA2828286152

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000243232

ClinVar Variation:

193596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Ser359Asn	CA239138 NM_001368144.1:c.1076G>A