Allele Registry

Canonical Allele Identifier: PA916035815

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000570714

RCV000692706

RCV002491136

ClinVar Variation:

485602

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Asn254Ser	CA398533958 NM_001353229.2:c.761A>G