Allele Registry

Canonical Allele Identifier: PA159775

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121103

RCV000228569

RCV000341795

RCV000569608

RCV001579897

RCV003935157

ClinVar Variation:

134426

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Asp198Asn	CA159773 NM_144997.7:c.592G>A