Allele Registry

Canonical Allele Identifier: PA213666

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029645

ClinVar Variation:

35988

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Met88Ile	CA213665 NM_000497.4:c.264G>A CA372396699 NM_000497.4:c.264G>C CA372396700 NM_000497.4:c.264G>T