Allele Registry

Canonical Allele Identifier: PA915957287

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029645

ClinVar Variation:

35988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Met88Ile	CA213665 NM_001026213.1:c.264G>A CA372396699 NM_001026213.1:c.264G>C CA372396700 NM_001026213.1:c.264G>T