Allele Registry

Canonical Allele Identifier: PA916035863

Gene: FLCN HGNC NCBI

ClinVar Allele:

327454

ClinVar RCV:

RCV000264762

RCV000319945

RCV000567800

RCV000589923

ClinVar Variation:

322065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Pro344Leu	CA8416182 NM_001353229.2:c.1031C>T