Allele Registry

Canonical Allele Identifier: PA159772

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121102

RCV000817735

RCV002255131

RCV003153396

ClinVar Variation:

134425

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Arg168Cys	CA159770 NM_144997.7:c.502C>T