Canonical Allele Identifier: PA2830263873
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2697836
ClinVar RCV Id: RCV003500982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu294_Glu295del
CA2636354613
NM_144997.7:c.880_885del