Allele Registry

Canonical Allele Identifier: PA2827720077

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000003536

RCV002512711

ClinVar Variation:

3369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340159.1:p.Ser79Trp	CA250446 NM_001353230.2:c.236C>G