Allele Registry

Canonical Allele Identifier: PA916035793

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121103

RCV000228569

RCV000341795

RCV000569608

RCV001579897

RCV003935157

ClinVar Variation:

134426

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Asp216Asn	CA159773 NM_001353229.2:c.646G>A