Canonical Allele Identifier: PA1139738251
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 993694
ClinVar RCV Id: RCV001812438 RCV002402810 RCV002541771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Met584Thr
CA8415916
NM_001353229.2:c.1751T>C