Allele Registry

Canonical Allele Identifier: PA2827719953

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 937384

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Gly34Arg	CA398535336 NM_001353230.2:c.100G>C CA398535337 NM_001353230.2:c.100G>A