Allele Registry

Canonical Allele Identifier: PA645426496

Gene: FLCN HGNC NCBI

ClinVar Allele:

242606

ClinVar RCV:

RCV000232477

RCV001024947

RCV002487093

ClinVar Variation:

241929

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Leu205Pro	CA10583456 NM_144997.7:c.614T>C