Allele Registry

Canonical Allele Identifier: PA2825669183

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001999400

ClinVar Variation:

1498831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001122062.3:p.Gly262Arg	CA3732560 NM_001128590.3:c.784G>C