Allele Registry

Canonical Allele Identifier: PA3057567434

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV004997895

ClinVar Variation:

3572103

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Val293Met	CA363511965 NM_001368144.1:c.877G>A