Canonical Allele Identifier: PA2827720781
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 822209
ClinVar RCV Id: RCV001017379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340159.1:p.Gln373Lys
CA8416137
NM_001353230.2:c.1117C>A