Canonical Allele Identifier: PA915957329
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_001021384.1:p.Thr318Arg
CA372395017
NM_001026213.1:c.953C>G