Allele Registry

Canonical Allele Identifier: PA916035776

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121102

RCV000817735

RCV002255131

RCV003153396

ClinVar Variation:

134425

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Arg186Cys	CA159770 NM_001353229.2:c.556C>T