Allele Registry

Canonical Allele Identifier: PA1139684066

Gene: CYP21A2 HGNC NCBI

ClinVar Allele:

976282

ClinVar RCV:

RCV001269617

ClinVar Variation:

988330

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Pro31Gln	CA363498902 NM_001128590.3:c.92C>A