Allele Registry

Canonical Allele Identifier: PA3063017154

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV005431322

ClinVar Variation:

3907234

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Leu174Phe	CA363507544 NM_001368144.1:c.520C>T