Canonical Allele Identifier: PA2827722042
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 643165
ClinVar RCV Id: RCV000796803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Glu308del
CA915949602
NM_001353231.2:c.922_924del