Canonical Allele Identifier: PA2827720612
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1483042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu305Lys
CA398533021
NM_001353230.2:c.913G>A