Allele Registry

Canonical Allele Identifier: PA645426441

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000467918

RCV001023971

RCV001198849

RCV001568283

RCV002480410

RCV003321612

ClinVar Variation:

409403

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Arg179Trp	CA8416388 NM_144997.7:c.535C>T