Allele Registry

Canonical Allele Identifier: PA658664424

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 485610

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Ala204Thr	CA398534186 NM_144997.7:c.610G>A