Canonical Allele Identifier: PA2827720877
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1020067
ClinVar RCV Id: RCV001319590 RCV002384409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Arg414Trp
CA398531783
NM_001353230.2:c.1240C>T