Canonical Allele Identifier: PA2830264834
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1447126
ClinVar RCV Id: RCV001996716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu544del
CA625014831
NM_144997.7:c.1632_1634del