Canonical Allele Identifier: PA916035772
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 460618
ClinVar RCV Id: RCV000553117 RCV001023371 RCV001574889 RCV002483392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Phe184Leu
CA288317129
NM_001353229.2:c.552C>G
CA398534425
NM_001353229.2:c.552C>A
CA398534430
NM_001353229.2:c.550T>C