Canonical Allele Identifier: PA2827719902
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1496182
ClinVar RCV Id: RCV002028451 RCV002486600 RCV003170480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg17Cys
CA8416533
NM_001353230.2:c.49C>T