Allele Registry

Canonical Allele Identifier: PA916035784

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000467918

RCV001023971

RCV001198849

RCV001568283

RCV002480410

RCV003321612

ClinVar Variation:

409403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Arg197Trp	CA8416388 NM_001353229.2:c.589C>T