Allele Registry

Canonical Allele Identifier: PA3057567427

Gene: CYP21A2 HGNC NCBI

ClinVar Allele:

3525531

ClinVar RCV:

RCV004771415

ClinVar Variation:

3366325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355073.1:p.Met105Thr	CA363505358 NM_001368144.1:c.314T>C