Allele Registry

Canonical Allele Identifier: PA2830263940

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 645979

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Arg320Trp	CA8416187 NM_144997.7:c.958C>T