Canonical Allele Identifier: PA2827720847
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2624774
ClinVar RCV Id: RCV003387006 RCV003607597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ile403Val
CA398531923
NM_001353230.2:c.1207A>G