Canonical Allele Identifier: PA2827720667
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2879645
ClinVar RCV Id: RCV003608507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Glu328Lys
CA398532877
NM_001353230.2:c.982G>A