Canonical Allele Identifier: PA2830264292
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1054815
ClinVar RCV Id: RCV001363392 RCV004036881
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Tyr405His
CA398531900
NM_144997.7:c.1213T>C