Canonical Allele Identifier: PA2580211241
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1721588
ClinVar RCV Id: RCV002302122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Trp278Gly
CA398533816
NM_001353229.2:c.832T>G