Allele Registry

Canonical Allele Identifier: PA916035899

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000121111

RCV000166127

RCV000231168

ClinVar Variation:

134431

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Val418Ile	CA159792 NM_001353229.2:c.1252G>A