Allele Registry

Canonical Allele Identifier: PA2827722230

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 840448

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340160.1:p.Val384Ile	CA8416132 NM_001353231.2:c.1150G>A