Allele Registry

Canonical Allele Identifier: PA3057317822

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

3525579

ClinVar RCV:

RCV004766488

ClinVar Variation:

3366374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Asp317Val	CA372395032 NM_001026213.1:c.950A>T