Allele Registry

Canonical Allele Identifier: PA100059

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121104

RCV000148504

RCV000163388

RCV000656850

RCV003945073

ClinVar Variation:

134427

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Arg239Cys	CA159776 NM_144997.7:c.715C>T