Canonical Allele Identifier: PA2830263869
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1057926
ClinVar RCV Id: RCV001367000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Asp291_Leu292delinsGlu
CA2499223918
NM_144997.7:c.873_875del