Canonical Allele Identifier: PA2827721292
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 819964
ClinVar RCV Id: RCV001231605 RCV001012941 RCV002481820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg578Gln
CA288303478
NM_001353230.2:c.1733G>A