Canonical Allele Identifier: PA645426643
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Tyr463His
CA8416012
NM_144997.7:c.1387T>C