Canonical Allele Identifier: PA1139737339
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 963725
ClinVar RCV Id: RCV001237794 RCV002375255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys327Glu
CA398532989
NM_001353229.2:c.979A>G