Allele Registry

Canonical Allele Identifier: PA645426646

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000321128

RCV000375788

RCV000571724

RCV003154723

ClinVar Variation:

322062

2445313

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Asp476Glu	CA8416006 NM_144997.7:c.1428C>G CA398531084 NM_144997.7:c.1428C>A