Canonical Allele Identifier: PA2830263980
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2059526
ClinVar RCV Id: RCV002952846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Ser331Tyr
CA398532854
NM_144997.7:c.992C>A