Canonical Allele Identifier: PA2741865161
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2956203
ClinVar RCV Id: RCV003813939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser349Cys
CA398532853
NM_001353229.2:c.1046C>G