Allele Registry

Canonical Allele Identifier: PA2828286067

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002481158

ClinVar Variation:

1809584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Val171Gly	CA363507470 NM_001368144.1:c.512T>G