Canonical Allele Identifier: PA2830263881
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2176197
ClinVar RCV Id: RCV002610128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Trp299Gly
CA8416198
NM_144997.7:c.895T>G