Allele Registry

Canonical Allele Identifier: PA096651

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

16210

ClinVar RCV:

RCV000001230

RCV000791917

RCV001199200

RCV002496223

ClinVar Variation:

1171

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg448His	CA339875 NM_000497.4:c.1343G>A