Allele Registry

Canonical Allele Identifier: PA2828286068

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211047

RCV002473356

ClinVar Variation:

1675318

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Phe172Val	CA3732571 NM_001368144.1:c.514T>G