Allele Registry

Canonical Allele Identifier: PA891849522

Gene: CYP21A2 HGNC NCBI

ClinVar Variation Id: 585755

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg17Cys	CA3732265 NM_000500.9:c.49C>T