Canonical Allele Identifier: PA2830263917
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 857899
ClinVar RCV Id: RCV001063666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Leu313Val
CA398532966
NM_144997.7:c.937T>G