Canonical Allele Identifier: PA2827719216
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2561012
ClinVar RCV Id: RCV003300734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ala6Thr
CA398535505
NM_001353229.2:c.16G>A