Allele Registry

Canonical Allele Identifier: PA2830284400

Gene: FLCN HGNC NCBI

ClinVar Allele:

138165

ClinVar RCV:

RCV000121103

RCV000228569

RCV000341795

RCV000569608

RCV001579897

RCV003935157

ClinVar Variation:

134426

HGVS (amino-acid)	Matching Registered Transcripts
NP_653207.1:p.Asp198Asn	CA159773 NM_144606.7:c.592G>A