Canonical Allele Identifier: PA2580211607
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1775692
ClinVar RCV Id: RCV002405802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Arg545Pro
CA398530445
NM_001353229.2:c.1634G>C