Canonical Allele Identifier: PA916035865
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 823563
ClinVar RCV Id: RCV001019912 RCV001346447 RCV001800930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Ser349Phe
CA8416177
NM_001353229.2:c.1046C>T