Canonical Allele Identifier: PA2827720627
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 579661
ClinVar RCV Id: RCV000703004 RCV001539928 RCV002369942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro311Leu
CA398532974
NM_001353230.2:c.932C>T