Canonical Allele Identifier: PA2580211418
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1742726
ClinVar RCV Id: RCV002335476
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Leu413Ile
CA398532006
NM_001353229.2:c.1237C>A