Canonical Allele Identifier: PA2827720062
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 3004139
ClinVar RCV Id: RCV003865778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro74Thr
CA398535074
NM_001353230.2:c.220C>A