Allele Registry

Canonical Allele Identifier: PA916035898

Gene: FLCN HGNC NCBI

ClinVar Allele:

467139

ClinVar RCV:

RCV000530248

RCV002350218

RCV002497102

ClinVar Variation:

460585

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Gly416Ala	CA8416100 NM_001353229.2:c.1247G>C