Canonical Allele Identifier: PA2830284070
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2842771
ClinVar RCV Id: RCV003608198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Glu70Val
CA398535098
NM_144606.7:c.209A>T