Canonical Allele Identifier: PA2830264730
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2091951
ClinVar RCV Id: RCV002991748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys514Glu
CA398530537
NM_144997.7:c.1540A>G