Canonical Allele Identifier: PA916035927
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485595
ClinVar RCV Id: RCV000571150 RCV000706666 RCV002281115 RCV002476247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.His447Asp
CA398531625
NM_001353229.2:c.1339C>G