Allele Registry

Canonical Allele Identifier: PA2827720969

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV001011104

RCV002298820

ClinVar Variation:

818969

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Ala445Ser	CA288305789 NM_001353230.2:c.1333G>T