Allele Registry

Canonical Allele Identifier: PA2573169781

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211047

RCV002473356

ClinVar Variation:

1675318

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Phe307Val	CA3732571 NM_000500.9:c.919T>G