Canonical Allele Identifier: PA2827720800
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1734040
ClinVar RCV Id: RCV002348881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Val384Phe
CA398532184
NM_001353230.2:c.1150G>T