Canonical Allele Identifier: PA2827719965
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1422865
ClinVar RCV Id: RCV001926295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Pro39Ser
CA398535299
NM_001353230.2:c.115C>T