Canonical Allele Identifier: PA2827720841
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 639998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg401His
CA8416095
NM_001353230.2:c.1202G>A