Allele Registry

Canonical Allele Identifier: PA645485015

Gene: CYP11B2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000269208

RCV000307908

RCV000366140

RCV000609130

RCV001275480

RCV001520473

RCV002488813

RCV003673319

ClinVar Variation:

362220

2797637

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Lys173Arg	CA4906184 NM_000498.3:c.518A>G CA2739269029 NM_000498.3:c.518_519delinsGA