Allele Registry

Canonical Allele Identifier: PA2830284468

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 485580

HGVS (amino-acid)	Matching Registered Transcripts
NP_653207.1:p.Ala225Thr	CA8416341 NM_144606.7:c.673G>A