Canonical Allele Identifier: PA2827722271
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 241914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Arg401Cys
CA8416096
NM_001353231.2:c.1201C>T