Allele Registry

Canonical Allele Identifier: PA2825669220

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000012963

ClinVar Variation:

12181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gly346Ser	CA3732653 NM_001128590.3:c.1036G>A