Canonical Allele Identifier: PA916035902
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 639998
ClinVar RCV Id: RCV000792931 RCV001010203 RCV003947983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg419His
CA8416095
NM_001353229.2:c.1256G>A