Allele Registry

Canonical Allele Identifier: PA2827719902

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 1496182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Arg17Cys	CA8416533 NM_001353230.2:c.49C>T