Canonical Allele Identifier: PA2827720819
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485590
ClinVar RCV Id: RCV000569998 RCV002528984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg392Gln
CA8416129
NM_001353230.2:c.1175G>A