Allele Registry

Canonical Allele Identifier: PA915957329

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

544735

ClinVar RCV:

RCV000672570

RCV001224692

ClinVar Variation:

556549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Thr318Arg	CA372395017 NM_001026213.1:c.953C>G