Allele Registry

Canonical Allele Identifier: PA645426636

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000223022

RCV000687348

RCV002485418

RCV003128597

ClinVar Variation:

230541

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Glu455Gly	CA8416016 NM_144997.7:c.1364A>G