Canonical Allele Identifier: PA2580211637
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778140
ClinVar RCV Id: RCV002414639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.His582Leu
CA398529840
NM_001353229.2:c.1745A>T