Canonical Allele Identifier: PA1139670585
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 908222
ClinVar RCV Id: RCV001158582 RCV001158583
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Asp268Asn
CA4905294
NM_001026213.1:c.802G>A