Canonical Allele Identifier: PA1139668109
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 909610
ClinVar RCV Id: RCV001160764 RCV001160765 RCV001160766 RCV004032847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Tyr266Asp
CA4906093
NM_000498.3:c.796T>G