Allele Registry

Canonical Allele Identifier: PA916035785

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000234368

RCV000523373

RCV001024230

RCV001125810

RCV002465599

ClinVar Variation:

241926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Asn202Lys	CA8416384 NM_001353229.2:c.606C>A CA398534303 NM_001353229.2:c.606C>G