Allele Registry

Canonical Allele Identifier: PA916036007

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 819901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Arg588Cys	CA8415912 NM_001353229.2:c.1762C>T