Allele Registry

Canonical Allele Identifier: PA2830264469

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV001350360

ClinVar Variation:

1045881

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Ala445Pro	CA398531442 NM_144997.7:c.1333G>C