Canonical Allele Identifier: PA916036002
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 485630
ClinVar RCV Id: RCV000561170 RCV001853772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys580Arg
CA8415917
NM_001353229.2:c.1739A>G