Canonical Allele Identifier: PA2830283907
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 993903
ClinVar RCV Id: RCV001297304 RCV001812962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Cys11Trp
CA398535465
NM_144606.7:c.33C>G