Canonical Allele Identifier: PA2827720844
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 646199
ClinVar RCV Id: RCV000800434 RCV002345786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Ile402Thr
CA398531930
NM_001353230.2:c.1205T>C