Allele Registry

Canonical Allele Identifier: PA2828285996

Gene: CYP21A2 HGNC NCBI

ClinVar RCV:

RCV000490344

RCV001357310

RCV003155127

ClinVar Variation:

225335

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355072.1:p.Ala257Thr	CA3732662 NM_001368143.1:c.769G>A