Canonical Allele Identifier: PA2499297840
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1016827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu12Lys
CA8416537
NM_144997.7:c.34G>A