Allele Registry

Canonical Allele Identifier: PA2827719272

Gene: FLCN HGNC NCBI

ClinVar Allele:

242613

ClinVar RCV:

RCV000229497

RCV000380278

RCV001027381

RCV002500821

RCV003151763

ClinVar Variation:

241932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340158.1:p.Pro28Ser	CA8416522 NM_001353229.2:c.82C>T