Canonical Allele Identifier: PA2580211611
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1775752
ClinVar RCV Id: RCV002398269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Pro546Leu
CA398530438
NM_001353229.2:c.1637C>T