Canonical Allele Identifier: PA1139756749
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 851074
ClinVar RCV Id: RCV001055395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Leu19Pro
CA398535419
NM_144997.7:c.56T>C