Canonical Allele Identifier: PA916035986
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 653093
ClinVar RCV Id: RCV000808791 RCV001292936 RCV002397657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Lys538Arg
CA8415935
NM_001353229.2:c.1613A>G