Allele Registry

Canonical Allele Identifier: PA645426464

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000234368

RCV000523373

RCV001024230

RCV001125810

RCV002465599

ClinVar Variation:

241926

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Asn184Lys	CA8416384 NM_144997.7:c.552C>A CA398534303 NM_144997.7:c.552C>G