Allele Registry

Canonical Allele Identifier: PA916035995

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000163471

RCV000231877

RCV001539507

RCV002267903

RCV002485010

ClinVar Variation:

184253

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Asp563Glu	CA188379 NM_001353229.2:c.1689C>G CA398529968 NM_001353229.2:c.1689C>A