Allele Registry

Canonical Allele Identifier: PA2573062932

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV003318405

ClinVar Variation:

1341485

HGVS (amino-acid)	Matching Registered Transcripts
NP_000491.4:p.Arg340His	CA3732614 NM_000500.9:c.1019G>A