Allele Registry

Canonical Allele Identifier: PA3057721341

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

4012087

ClinVar RCV:

RCV005409121

ClinVar Variation:

3896216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Thr318Pro	CA372395022 NM_001026213.1:c.952A>C