Allele Registry

Canonical Allele Identifier: PA2827722399

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV001350360

ClinVar Variation:

1045881

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340160.1:p.Ala445Pro	CA398531442 NM_001353231.2:c.1333G>C