Allele Registry

Canonical Allele Identifier: PA916035817

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121104

RCV000148504

RCV000163388

RCV000656850

RCV003945073

ClinVar Variation:

134427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Arg257Cys	CA159776 NM_001353229.2:c.769C>T