Canonical Allele Identifier: PA2830264208
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_659434.2:p.Val384Phe
CA398532184
NM_144997.7:c.1150G>T