Allele Registry

Canonical Allele Identifier: PA658664435

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000570714

RCV000692706

RCV002491136

ClinVar Variation:

485602

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Asn236Ser	CA398533958 NM_144997.7:c.707A>G