Canonical Allele Identifier: PA916036012
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_001340158.1:p.Arg596Gln
CA288303478
NM_001353229.2:c.1787G>A