Canonical Allele Identifier: PA2827720741
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 581992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Leu356Val
CA8416144
NM_001353230.2:c.1066C>G