Canonical Allele Identifier: PA2827719392
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1786234
ClinVar RCV Id: RCV002417611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser71Pro
CA8416493
NM_001353229.2:c.211T>C