Canonical Allele Identifier: PA2830264235
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1739975
ClinVar RCV Id: RCV002332312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Leu391Pro
CA398532102
NM_144997.7:c.1172T>C