Canonical Allele Identifier: PA2827720665
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1021589
ClinVar RCV Id: RCV001321380 RCV002377400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ala327Thr
CA398532885
NM_001353230.2:c.979G>A