Allele Registry

Canonical Allele Identifier: PA096730

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001237

RCV001781159

RCV002247232

RCV002496224

ClinVar Variation:

1178

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Thr319Met	CA339881 NM_000497.4:c.956C>T