Allele Registry

Canonical Allele Identifier: PA2828286063

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001999400

ClinVar Variation:

1498831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Gly157Arg	CA3732560 NM_001368144.1:c.469G>C