Canonical Allele Identifier: PA645426636
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 230541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu455Gly
CA8416016
NM_144997.7:c.1364A>G