Allele Registry

Canonical Allele Identifier: PA913194510

Gene: CYP21A2 HGNC NCBI

ClinVar Variation Id: 596309

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Pro483Ser	CA3732730 NM_000500.9:c.1447C>T