Allele Registry

Canonical Allele Identifier: PA916035923

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000163906

RCV000529447

RCV001544699

RCV002492651

ClinVar Variation:

184619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Pro446His	CA189480 NM_001353229.2:c.1337C>A