Canonical Allele Identifier: PA2499251411
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 1057926
ClinVar RCV Id: RCV001367000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340158.1:p.Asp309_Leu310delinsGlu
CA2499223918
NM_001353229.2:c.927_929del