Canonical Allele Identifier: PA2830263902
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 963724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu307Val
CA398533001
NM_144997.7:c.920A>T