Canonical Allele Identifier: PA096708
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 556549
ClinVar RCV Id: RCV000672570 RCV001224692
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Thr318Arg
CA372395017
NM_000497.4:c.953C>G