Allele Registry

Canonical Allele Identifier: PA2827721392

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000469363

RCV001017432

RCV001558005

RCV001844165

RCV002489056

RCV003409629

ClinVar Variation:

409391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340160.1:p.Ser38Ile	CA8416514 NM_001353231.2:c.113G>T