Canonical Allele Identifier: PA2830284009
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 187016
ClinVar RCV Id: RCV000166697 RCV000465657 RCV002492672 RCV002280106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653207.1:p.Glu47Gln
CA196505
NM_144606.7:c.139G>C