Canonical Allele Identifier: PA2827720644
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1767285
ClinVar RCV Id: RCV002374246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu318Gln
CA398532935
NM_001353230.2:c.952G>C