Canonical Allele Identifier: PA2827722029
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2176197
ClinVar RCV Id: RCV002610128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340160.1:p.Trp299Gly
CA8416198
NM_001353231.2:c.895T>G