Canonical Allele Identifier: PA916035954
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 409380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Tyr481His
CA8416012
NM_001353229.2:c.1441T>C