Allele Registry

Canonical Allele Identifier: PA658664433

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000560997

RCV001059272

RCV002491135

ClinVar Variation:

485580

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Ala225Thr	CA8416341 NM_144997.7:c.673G>A