Allele Registry

Canonical Allele Identifier: PA159794

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121111

RCV000166127

RCV000231168

ClinVar Variation:

134431

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Val400Ile	CA159792 NM_144997.7:c.1198G>A