Allele Registry

Canonical Allele Identifier: PA645426567

Gene: FLCN HGNC NCBI

ClinVar Allele:

327454

ClinVar RCV:

RCV000264762

RCV000319945

RCV000567800

RCV000589923

ClinVar Variation:

322065

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Pro326Leu	CA8416182 NM_144997.7:c.977C>T