Allele Registry

Canonical Allele Identifier: PA2827722188

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000564803

RCV000691604

RCV001127833

RCV002483536

RCV003321681

RCV003409849

RCV003478283

ClinVar Variation:

485585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340160.1:p.Arg362Cys	CA8416141 NM_001353231.2:c.1084C>T