Allele Registry

Canonical Allele Identifier: PA645426359

Gene: FLCN HGNC NCBI

ClinVar RCV:

RCV000229497

RCV000380278

RCV001027381

RCV002500821

RCV003151763

ClinVar Variation:

241932

HGVS (amino-acid)	Matching Registered Transcripts
NP_659434.2:p.Pro28Ser	CA8416522 NM_144997.7:c.82C>T