Allele Registry

Canonical Allele Identifier: PA2830264257

Gene: FLCN HGNC NCBI

ClinVar Variation Id: 858638

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Met394Thr	CA398532013 NM_144997.7:c.1181T>C