Allele Registry

Canonical Allele Identifier: PA100082

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000567009

RCV000812782

RCV001755958

RCV002497214

ClinVar Variation:

485611

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.His429Tyr	CA8416073 NM_144997.7:c.1285C>T