Allele Registry

Canonical Allele Identifier: PA916035963

Gene: FLCN HGNC NCBI

ClinVar Allele:

327448

ClinVar RCV:

RCV000266163

RCV000379332

RCV000414396

RCV000765332

RCV001011546

ClinVar Variation:

322061

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Arg495Gln	CA8416005 NM_001353229.2:c.1484G>A