Allele Registry

Canonical Allele Identifier: PA096793

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000272288

RCV000321492

RCV000357616

RCV000949532

RCV002158743

ClinVar Variation:

242772

1653091

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Val386Ala	CA038824 NM_000498.3:c.1157T>C CA038861 NM_000498.3:c.[1157T>C;541C>T] CA038927 NM_000498.3:c.[1157T>C;594A>C] CA2573142869 NM_000498.3:c.1157_1158delinsCA