Allele Registry

Canonical Allele Identifier: PA2573169778

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV001999400

ClinVar Variation:

1498831

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Gly292Arg	CA3732560 NM_000500.9:c.874G>C