Allele Registry

Canonical Allele Identifier: PA916035961

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000321128

RCV000375788

RCV000571724

RCV003154723

ClinVar Variation:

322062

2445313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Asp494Glu	CA8416006 NM_001353229.2:c.1482C>G CA398531084 NM_001353229.2:c.1482C>A