Allele Registry

Canonical Allele Identifier: PA2573169779

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV002211046

RCV002281650

ClinVar Variation:

1675317

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Val305Met	CA3732569 NM_000500.9:c.913G>A