Canonical Allele Identifier: PA645426600
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Arg401Cys
CA8416096
NM_144997.7:c.1201C>T