Canonical Allele Identifier: PA2827719239
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1744659
ClinVar RCV Id: RCV002343009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg17Ser
CA398535432
NM_001353229.2:c.49C>A