Allele Registry

Canonical Allele Identifier: PA2827720801

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 840448

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Val384Ile	CA8416132 NM_001353230.2:c.1150G>A